Evidence map›Paper›PMID 40893959›Full record

ArticleACS central science2025

Generative Landscapes and Dynamics to Design Functional Multidomain Artificial Transmembrane Transporters.

Fernando Montalvillo Ortega, Fariha Hossain, Vladimir V Volobouev, Gabriele Meloni, Hedieh Torabifard, Faruck Morcos

Abstract read
In one paragraph

Article in ACS central science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 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. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Fernando Montalvillo OrtegaDepartment of Chemistry and Biochemistry, University of Texas at Dallas, Richardson, 75080 Texas, United States.ORCID https://orcid.org/0009-0008-5041-9930
Fariha HossainDepartment of Biological Sciences, University of Texas at Dallas, Richardson, 75080 Texas, United States.
Vladimir V VolobouevDepartment of Biological Sciences, University of Texas at Dallas, Richardson, 75080 Texas, United States.
Gabriele MeloniDepartment of Chemistry and Biochemistry, University of Texas at Dallas, Richardson, 75080 Texas, United States.ORCID https://orcid.org/0000-0003-4976-1401
Hedieh TorabifardDepartment of Chemistry and Biochemistry, University of Texas at Dallas, Richardson, 75080 Texas, United States.ORCID https://orcid.org/0000-0003-0687-6858
Faruck MorcosDepartment of Biological Sciences, University of Texas at Dallas, Richardson, 75080 Texas, United States.ORCID https://orcid.org/0000-0001-6208-1561

Funding

Principles of selectivity and translocation in transition metal transporters, metallochaperones, and associated metalloproteinsR35GM128704 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI Gabriele Meloni · 2018 to 2026
$3.5M
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
Computational framework to investigate the inorganic ion transportersR35GM155106 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI Hedieh Torabifard · 2024 to 2026
$1.2M
NIGMS NIH HHS R35 GM128704NIGMS NIH HHS R35 GM133631NIGMS NIH HHS R35 GM155106
6 · The paper itself

Abstract

Design and synthesis of functionally active artificial proteins is challenging, as it requires simultaneous consideration of interconnected factors, such as fold, dynamics, and function. These evolutionary constraints are encoded in protein sequences and can be learned through the latent generative landscape (LGL) framework to predict functional sequences by leveraging evolutionary patterns, enabling exploration of uncharted sequence space. By simulating designed proteins through molecular dynamics (MD), we gain deeper insights into the interdependencies governing structure and dynamics. We present a synergized workflow combining LGL with MD and biochemical characterization, allowing us to explore the sequence space effectively. This approach has been applied to design and characterize two artificial multidomain ATP-driven transmembrane copper transporters, with native-like functionality. This integrative approach proved effective in revealing the intricate relationships between sequence, structure, and function.

Identifiers

PMID40893959
PMCPMC12395301

What OpenQuestion holds

Textmetadata
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.