Evidence map›Paper›PMID 37076519›Full record

ArticleNature communications2023

Latent generative landscapes as maps of functional diversity in protein sequence space.

Cheyenne Ziegler, Jonathan Martin, Claude Sinner, Faruck Morcos

Abstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. A structure-aware generative AI framework for revealing functional relationships in protein families.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Leveraging latent space models for enzyme discovery and sampling.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
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  7. INBAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  17. Bioengineering hybrid artificial life.Frontiers in bioinformatics · 2025
    Review
  18. Article
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  20. Machine learning in biological physics: From biomolecular prediction to design.Proceedings of the National Academy of Sciences of the United States of America · 2024
    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.

Cheyenne Ziegler *Department of Biological Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0002-6379-3162
Jonathan Martin *Department of Biological Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.ORCID 0000-0003-0946-3864
Claude SinnerDepartment of Biological Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA.
Faruck MorcosDepartment of Biological Sciences, University of Texas at Dallas, Richardson, TX, 75080, USA. faruckm@utdallas.edu.ORCID 0000-0001-6208-1561

Funding

Computational Tools to Characterize the Effects of Protein and RNA Variability in Function and InteractionsR35GM133631 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI Alonso Faruck Morcos · 2019 to 2026
$3.0M
NIGMS NIH HHS R35 GM133631NIH HHS R35GM133631
6 · The paper itself

Abstract

Variational autoencoders are unsupervised learning models with generative capabilities, when applied to protein data, they classify sequences by phylogeny and generate de novo sequences which preserve statistical properties of protein composition. While previous studies focus on clustering and generative features, here, we evaluate the underlying latent manifold in which sequence information is embedded. To investigate properties of the latent manifold, we utilize direct coupling analysis and a Potts Hamiltonian model to construct a latent generative landscape. We showcase how this landscape captures phylogenetic groupings, functional and fitness properties of several systems including Globins, β-lactamases, ion channels, and transcription factors. We provide support on how the landscape helps us understand the effects of sequence variability observed in experimental data and provides insights on directed and natural protein evolution. We propose that combining generative properties and functional predictive power of variational autoencoders and coevolutionary analysis could be beneficial in applications for protein engineering and design.

Indexed as

GlobinsTranscription FactorsAmino Acid Sequencebeta-LactamasesPhylogenybeta-LactamasesGlobinsTranscription Factors

Identifiers

PMID37076519
PMCPMC10113739

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.