Evidence map›Paper›PMID 42818380›Full record

ArticlebioRxiv : the preprint server for biology2026

Substrate Binding Relieves Autoinhibition of the Mammalian GCN2 Kinase.

Marco A Catipovic, Rachel Green

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

2 authors.

Marco A CatipovicDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine; Baltimore, MD, 21205, United States of America.ORCID 0000-0001-6766-829X
Rachel GreenDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine; Baltimore, MD, 21205, United States of America.ORCID 0000-0001-9337-2003

Funding

Molecular mechanisms of ribosome-mediated kinase signalingR35GM156244 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI GREEN, RACHEL · 2025 to 2025
$2.1M
NIGMS NIH HHS R35 GM156244
6 · The paper itself

Abstract

Cells respond to amino acid starvation and translational stress through the integrated stress response (ISR) kinase GCN2. Current models maintain that GCN2 senses these stresses either by binding deacylated tRNAs that accumulate during amino acid starvation or by recognizing ribosome collisions that arise from perturbation of translation elongation. As tRNA charging is inherently coupled to translation elongation, assessing the relative contributions of these two pathways has proven difficult. To fully separate the roles of these potential agonists, we reconstituted the regulation of GCN2

Identifiers

PMID42818380
PMCPMC13622680

What OpenQuestion holds

Textmetadata
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.