Evidence map›Paper›PMID 28606055›Full record

ArticleBMC evolutionary biology2017

Improved mitochondrial amino acid substitution models for metazoan evolutionary studies.

Vinh Sy Le, Cuong Cao Dang, Quang Si Le

Abstract read
In one paragraph

Article in BMC evolutionary biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

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0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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.

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Article
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  5. Review
  6. The complete mitochondrial genome of a wild-collectedMitochondrial DNA. Part B, Resources · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. FLAVI: An Amino Acid Substitution Model for Flaviviruses.Journal of molecular evolution · 2020
    Article
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  12. 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

3 authors.

Vinh Sy LeUniversity of Engineering and Technology, Vietnam National University Hanoi, Hanoi, Vietnam. vinhls@vnu.edu.vn.
Cuong Cao DangUniversity of Engineering and Technology, Vietnam National University Hanoi, Hanoi, Vietnam.
Quang Si LeSchool of Pharmacy and Biomedical Sciences, University of Portsmouth, Winston Churchill Avenue Portsmouth, Portsmouth, PO1 2UP, UK. lsquang@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmino acid substitution models play an essential role in inferring phylogenies from mitochondrial protein data. However, only few empirical models have been estimated from restricted mitochondrial protein data of a hundred species. The existing models are unlikely to represent appropriately the amino acid substitutions from hundred thousands metazoan mitochondrial protein sequences.

resultsWe selected 125,935 mitochondrial protein sequences from 34,448 species in the metazoan kingdom to estimate new amino acid substitution models targeting metazoa, vertebrates and invertebrate groups. The new models help to find significantly better likelihood phylogenies in comparison with the existing models. We noted remarkable distances from phylogenies with the existing models to the maximum likelihood phylogenies that indicate a considerable number of incorrect bipartitions in phylogenies with the existing models. Finally, we used the new models and mitochondrial protein data to certify that Testudines, Aves, and Crocodylia form one separated clade within amniotes.

conclusionsWe introduced new mitochondrial amino acid substitution models for metazoan mitochondrial proteins. The new models outperform the existing models in inferring phylogenies from metazoan mitochondrial protein data. We strongly recommend researchers to use the new models in analysing metazoan mitochondrial protein data.

Indexed as

Models, GeneticPhylogenyAmino Acid SubstitutionAnimalsEvolution, MolecularHumansInvertebratesMitochondriaMitochondrial ProteinsSequence Homology, Amino AcidVertebratesMitochondrial ProteinsInvertebratesMetazoaMitochondrial amino acid substitution modelsVertebrates

Identifiers

PMID28606055
PMCPMC5469158

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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.