Evidence map›Paper›PMID 38570624›Full record

ArticleScientific reports2024

Phylogeny and structural modeling of the transcription factor CsqR (YihW) from Escherichia coli.

Anna A Rybina, Roman A Glushak, Tatiana A Bessonova, Artemiy I Dakhnovets, Alexander Yu Rudenko, Ratislav M Ozhiganov, Anna D Kaznadzey, Maria N Tutukina, Mikhail S Gelfand

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. 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
0.6field-weighted citation impact, top 30% of its field
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 citations in OpenAlex.

  1. Sulfoquinovose Catabolism inInternational journal of molecular sciences · 2025
    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 at 4 institutions in 1 country.

Anna A RybinaSkolkovo Institute of Science and Technology, Moscow, Russia, 121205. rybinaann@gmail.com.
Roman A GlushakFaculty of Biology, Lomonosov Moscow State University, Moscow, Russia, 119234.
Tatiana A BessonovaInstitute of Cell Biophysics RAS (Federal Research Center "Pushchino Scientific Center for Biological Research RAS"), Pushchino, Russia, 142290.
Artemiy I DakhnovetsSkolkovo Institute of Science and Technology, Moscow, Russia, 121205.
Alexander Yu RudenkoBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia, 119991.
Ratislav M OzhiganovBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia, 119991.
Anna D KaznadzeyInstitute for Information Transmission Problems RAS, Moscow, Russia, 127051.
Maria N TutukinaSkolkovo Institute of Science and Technology, Moscow, Russia, 121205.
Mikhail S GelfandSkolkovo Institute of Science and Technology, Moscow, Russia, 121205.
Lomonosov Moscow State University · RUSkolkovo Institute of Science and Technology · RUInstitute of Cell Biophysics · RUInstitute for Information Transmission Problems · RU

Funding

Russian Foundation for Basic Research 20-54-14005
6 · The paper itself

Abstract

CsqR (YihW) is a local transcription factor that controls expression of yih genes involved in degradation of sulfoquinovose in Escherichia coli. We recently showed that expression of the respective gene cassette might be regulated by lactose. Here, we explore the phylogenetic and functional traits of CsqR. Phylogenetic analysis revealed that CsqR had a conserved Met25. Western blot demonstrated that CsqR was synthesized in the bacterial cell as two protein forms, 28.5 (CsqR-l) and 26 kDa (CsqR-s), the latter corresponding to start of translation at Met25. CsqR-s was dramatically activated during growth with sulfoquinovose as a sole carbon source, and displaced CsqR-l in the stationary phase during growth on rich medium. Molecular dynamic simulations revealed two possible states of the CsqR-s structure, with the interdomain linker being represented by either a disordered loop or an ɑ-helix. This helix allowed the hinge-like motion of the N-terminal domain resulting in a switch of CsqR-s between two conformational states, "open" and "compact". We then modeled the interaction of both CsqR forms with putative effectors sulfoquinovose, sulforhamnose, sulfoquinovosyl glycerol, and lactose, and revealed that they all preferred the same pocket in CsqR-l, while in CsqR-s there were two possible options dependent on the linker structure.

Indexed as

Escherichia coliEscherichia coli ProteinsLactosePhylogenyTranscription FactorsEscherichia coli ProteinsLactoseTranscription Factors

Identifiers

PMID38570624
PMCPMC10991401
OpenAlexW4393850068

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.