Evidence map›Paper›PMID 42367944›Full record

ArticlebioRxiv : the preprint server for biology2026

GTRspmix: Capturing Heterogeneity of Exchangeabilities Across Sites to Improve Protein Phylogenetics.

Ryo Harada, Edward Susko, Thomas K F Wong, Hector Baños, Nhan Ly-Trong, Robert Lanfear, Douglas L Theobald, Bui Quang Minh, Andrew J Roger

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Ryo HaradaInstitute for Comparative Genomics, Dalhousie University, Halifax, NS, B3H 4R2, Canada.ORCID 0000-0003-4883-5341
Edward SuskoInstitute for Comparative Genomics, Dalhousie University, Halifax, NS, B3H 4R2, Canada.ORCID 0000-0003-1122-8740
Thomas K F WongSchool of Computing, College of Systems and Society, Australian National University, Canberra, ACT, 2601, Australia.ORCID 0000-0002-0580-6324
Hector BañosDepartment of Mathematics, California State University San Bernardino, San Bernardino, CA, 92407, USA.ORCID 0000-0001-5769-2544
Nhan Ly-TrongSchool of Computing, College of Systems and Society, Australian National University, Canberra, ACT, 2601, Australia.ORCID 0000-0001-5668-5027
Robert LanfearResearch School of Biology, College of Science and Medicine, Australian National University, Canberra, ACT, 2601, Australia.ORCID 0000-0002-1140-2596
Douglas L TheobaldDepartment of Biochemistry, Brandeis University, Waltham, MA, 02453, USA.ORCID 0000-0002-2695-8343
Bui Quang MinhSchool of Computing, College of Systems and Society, Australian National University, Canberra, ACT, 2601, Australia.ORCID 0000-0002-5535-6560
Andrew J RogerInstitute for Comparative Genomics, Dalhousie University, Halifax, NS, B3H 4R2, Canada.ORCID 0000-0003-1370-9820

Funding

Evolution of enzyme structure and function viewed at atomic resolutionR01GM096053 · NIGMS · BRANDEIS UNIVERSITY · PI Douglas Lowell Theobald · 2011 to 2026
$3.6M
Empirically testing the accuracy and bias of ancestral protein resurrection methodsR01GM132499 · NIGMS · BRANDEIS UNIVERSITY · PI THEOBALD, DOUGLAS LOWELL · 2019 to 2022
$1.4M
NIGMS NIH HHS R01 GM096053NIGMS NIH HHS R01 GM132499
6 · The paper itself

Abstract

Site rate and profile mixture models capture the heterogeneity of the amino acid substitution process across sites. However, these models typically use a single matrix of amino acid exchangeabilities and ignore potential heterogeneities of these exchangeabilities across sites. Simply combining multiple exchangeability matrices with rate and profile mixtures leads to a combinatorial explosion of mixture components and a prohibitive increase in free parameters. Here, we introduce GTRspmix, a novel framework that incorporates multiple exchangeability matrices into profile and site rate mixture models while effectively managing model complexity. GTRspmix employs a clustering-based strategy that groups profiles and assigns a distinct exchangeability matrix to each profile cluster. Evaluations using both empirical and simulated datasets demonstrate that GTRspmix fits empirical data significantly better than conventional models, and that overparameterization does not present a problem for sufficiently large alignments. Based on these results, we estimated general-purpose empirical models (SXXpfamCYY series available in IQ-TREE3) from the Pfam database. These general-purpose models not only fit data much better, but they also influence branch length and tree topology estimates, effectively mitigating long-branch attraction artifacts. Because the total number of rate matrices remains manageable, the computational efficiency of the inference is identical to that of conventional profile mixture models (e.g., LG+C60+G4). GTRspmix provides a more realistic and flexible model of protein evolution, offering a robust foundation for the inference of reliable phylogenetic trees.

Indexed as

Exchangeability heterogeneityGTRspmixIQ-TREEMaximum likelihoodMixture modelsPhylogenomics

Identifiers

PMID42367944
PMCPMC13308233

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.