Evidence map›Paper›PMID 40721149›Full record

ArticleJournal of molecular biology2025

Sequence Determinants of Allosteric Back-to-front Control of the Arf Nucleotide Switch.

Noam Hantman, Tejaswi Koduru, Edgar V Peters, Michel W Jaworek, Scott A McCallum, Richard E Gillilan, Roland Winter, Jacqueline Cherfils, Catherine A Royer

Abstract read
In one paragraph

Article in Journal of molecular biology, 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. Article
  2. 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

9 authors.

Noam HantmanGraduate Program in Biochemistry and Biophysics, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.
Tejaswi KoduruDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.
Edgar V PetersDepartment of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.
Michel W JaworekDepartment of Chemistry and Chemical Biology, Biophysical Chemistry, TU Dortmund University, D-44227 Dortmund, Germany.
Scott A McCallumShirley Ann Jackson, PhD. Center for Biotechnology and Interdisciplinary Science, Rensselaer Polytechnic Institute, Troy, NY 12180, United States.
Richard E GillilanCornell High Energy Synchrotron Source, Cornell University, Ithaca, NY 14853, United States.
Roland WinterDepartment of Chemistry and Chemical Biology, Biophysical Chemistry, TU Dortmund University, D-44227 Dortmund, Germany.
Jacqueline CherfilsUniversité Paris-Saclay, Ecole Normale Supérieure Paris-Saclay, CNRS, 91190 Gif-sur-Yvette, France.
Catherine A RoyerDepartment of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY 12180, United States. Electronic address: royerc@rpi.edu.

Funding

Training and OutreachP30GM124166 · NIGMS · CORNELL UNIVERSITY · PI RICHARD A. CERIONE · 2019 to 2026
$28.3M
Arf Functional LandscapesR01GM137766 · NIGMS · RENSSELAER POLYTECHNIC INSTITUTE · PI ROYER, CATHERINE A · 2020 to 2024
$1.7M
Regional 800 MHz NMR System UpgradeS10OD030482 · OD · RENSSELAER POLYTECHNIC INSTITUTE · PI MONTELIONE, GAETANO T · 2021 to 2021
$1.3M
NIGMS NIH HHS P30 GM124166NIGMS NIH HHS R01 GM137766NIH HHS S10 OD030482
6 · The paper itself

Abstract

Unlike AI-based protein structure prediction, the sequence determinants of protein dynamics, and thus function, remain elusive. The nucleotide switch in Arf GTPases involves a massive structural change, which we showed recently in Arf1 is facilitated by a dynamic molten globule ensemble. Here we investigate the unresolved sequence-dynamics paradigm by comparing Arf1 and Arf6 using a combination of high-pressure NMR and other biophysical methods. We show that, as for Arf1, the Arf6 nucleotide switch implicates a functional molten globule ensemble, suggesting that this mechanism is a general feature of Arf and Arf-like GTPases. Comparison of the local stability distributions identifies key sequence determinants for the differences in switching between Arf1 and Arf6. Remarkably, these determinants are distant from the nucleotide-binding site, revealing back-to-front allosteric coupling controlling the switch. Evolutionary covariance analysis suggests that this back-to-front allosteric coupling is a fundamental characteristic of the Arf and Arf-like family, and may extend to the entire small GTPase kingdom. Our study thus establishes notable sequence-dynamics relationships with implications for signaling and diseases.

Indexed as

ADP-Ribosylation Factor 1ADP-Ribosylation FactorsNucleotidesADP-Ribosylation Factor 6Allosteric RegulationAmino Acid SequenceBinding SitesHumansModels, MolecularProtein ConformationADP-Ribosylation Factor 1ADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF1 protein, humanARF6 protein, humanNucleotidesallosteryArf GTPaseshigh pressureNMRSAXS

Identifiers

PMID40721149
PMCPMC12355652

What OpenQuestion holds

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Registered trials

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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.