Evidence map›Paper›PMID 40396811›Full record

ReviewChembiochem : a European journal of chemical biology2025

Methods for Controlling Small GTPase Activity.

Benjamin Faulkner, Yuchen He, Daniel Sitrin, Cliff I Stains

Abstract readReview
In one paragraph

Review in Chembiochem : a European journal of chemical 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

4 authors.

Benjamin FaulknerDepartment of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
Yuchen HeDepartment of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
Daniel SitrinDepartment of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.
Cliff I StainsDepartment of Chemistry, University of Virginia, Charlottesville, VA, 22904, USA.ORCID https://orcid.org/0000-0002-3165-4539

Funding

Chemical Approaches for Interrogating Fundamental Biomedical ProcessesR35GM148221 · NIGMS · UNIVERSITY OF VIRGINIA · PI Cliff I Stains · 2023 to 2026
$1.6M
NIGMS NIH HHS R35 GM148221NIH HHS R35GM148221
6 · The paper itself

Abstract

Small GTPases comprise a diverse class of signaling proteins in mammalian cells and regulate a variety of cellular processes such as cell growth, cell movement, vesicle formation, and nuclear transport. Due to their involvement in critical cellular pathways, changes in the activation state of small GTPases due to genetic mutations or alterations in gene expression can lead to human diseases. As such, the ability to control the activity of small GTPases is paramount in understanding the precise role these proteins play in human biology and in reducing their impacts on related diseases. Herein, important advances made in the development of small-molecule- and protein engineering-based strategies to control the activity of small GTPases are presented. Current approaches within each area are discussed within their historical contexts along with commentary on the importance that each technology has had on improving the ability to regulate small GTPase activity. Given this ever-evolving toolbox for controlling small GTPase signaling, continued growth in the study of this protein class is anticipated.

Indexed as

Monomeric GTP-Binding ProteinsSmall Molecule LibrariesAnimalsHumansProtein EngineeringSignal TransductionMonomeric GTP-Binding ProteinsSmall Molecule Librariesinhibitorsprotein engineeringsignal transductionssmall GTPasessplit proteins

Identifiers

PMID40396811
PMCPMC12247031

What OpenQuestion holds

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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.