Evidence map›Paper›PMID 41607018›Full record

ArticleAngewandte Chemie (International ed. in English)2026

Targeting the Membrane-Embedded Rhomboid Protease GlpG: A Multimodal Strategy for Inhibitor Discovery and Mechanistic Insight.

Claudia Bohg, Yurii Dubanych, Spyridon Kosteletos, Taoran Xiao, Martin Neuenschwander, Tillmann Utesch, Michael Lisurek, Carl Öster, Andreas Oder, Carola Seyffarth and 12 more

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

22 authors.

Claudia BohgResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.ORCID 0000-0003-0793-3199
Yurii DubanychInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Spyridon KosteletosResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Taoran XiaoResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Martin NeuenschwanderCore Facility Screening Unit, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Tillmann UteschResearch Unit Structural Chemistry & Computational Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Michael LisurekResearch Unit Structural Chemistry & Computational Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Carl ÖsterResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Andreas OderCore Facility Screening Unit, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Carola SeyffarthCore Facility Screening Unit, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Kathrin BachInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Denise-Liù Gracias LeoneInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
František FilandrInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Marc WegertResearch Unit Biomolecule Modification and Delivery, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Sascha LangeResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Henry SawczycResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Jens Peter von KriesCore Facility Screening Unit, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Christian P R HackenbergerResearch Unit Biomolecule Modification and Delivery, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Edgar SpeckerCore Facility Compound Management, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Han SunResearch Unit Structural Chemistry & Computational Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.
Kvido StříšovskýInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Adam LangeResearch Unit Molecular Biophysics, Leibniz Forschungsinstitut für Molekulare Pharmakologie (FMP), Berlin, Germany.ORCID 0000-0002-7534-5973

Funding

Deutsche ForschungsgemeinschaftMinistry of Education, Youth and Sports of the Czech Republic LUC23180
6 · The paper itself

Abstract

Rhomboid proteases, a class of intramembrane proteases characterized by a Ser-His catalytic dyad, have recently emerged as promising therapeutic targets. While inhibitors for soluble serine proteases have been extensively studied, the spectrum of potent rhomboid protease inhibitor chemotypes is limited to active-site targeted nucleophiles. To address this limitation, we conducted a high-throughput screen of over 68,000 compounds targeting the E. coli rhomboid protease GlpG, using a fluorescent liposome-based assay. A selection of 326 inhibitory compounds was evaluated in a subsequent IC

Indexed as

DNA-Binding ProteinsDrug DiscoveryEndopeptidasesEscherichia coli ProteinsMembrane ProteinsMitochondrial ProteinsProtease InhibitorsEscherichia coliHumansMolecular Docking SimulationDNA-Binding ProteinsEndopeptidasesEscherichia coli ProteinsGlpG protein, E coliMembrane ProteinsMitochondrial ProteinsProtease Inhibitorsdrug discoveryhigh‐throughput screeningintramembrane proteolysismembrane enzymesprotein drug interactions

Identifiers

PMID41607018
PMCPMC12955534

What OpenQuestion holds

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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.