Evidence map›Paper›PMID 32356522›Full record

ArticleActa crystallographica. Section F, Structural biology communications2020

Crystal structure of the nucleoid-associated protein Fis (PA4853) from Pseudomonas aeruginosa.

Juan Zhou, Zengqiang Gao, Heng Zhang, Yuhui Dong

Open access · greenAbstract read
In one paragraph

Article in Acta crystallographica. Section F, Structural biology communications, 2020. 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, top 97% 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

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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. 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 at 2 institutions in 1 country.

Juan ZhouInstitute of Health Sciences and School of Life Science, Anhui University, Hefei, Anhui 230601, People's Republic of China.
Zengqiang GaoBeijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, People's Republic of China.
Heng ZhangBeijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, People's Republic of China.
Yuhui DongBeijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049, People's Republic of China.ORCID 0000-0002-4422-4685
Chinese Academy of Sciences · CNAnhui University · CN

Funding

Chinese Academy of Sciences, Strategic Priority Research Program XDB08030103National Basic Research Program of China (973 Program) 2017YFA0504900National Natural Science Foundation of China 31570744)National Natural Science Foundation of China 31670059National Natural Science Foundation of China U1732113
6 · The paper itself

Abstract

Factor for inversion stimulation (Fis) is a versatile bacterial nucleoid-associated protein that can directly bind and bend DNA to influence DNA topology. It also plays crucial roles in regulating bacterial virulence factors and in optimizing bacterial adaptation to various environments. Fis from Pseudomonas aeruginosa (PA4853, referred to as PaFis) has recently been found to be required for virulence by regulating the expression of type III secretion system (T3SS) genes. PaFis can specifically bind to the promoter region of exsA, which functions as a T3SS master regulator, to regulate its expression and plays an essential role in transcription elongation from exsB to exsA. Here, the crystal structure of PaFis, which is composed of a four-helix bundle and forms a homodimer, is reported. PaFis shows remarkable structural similarities to the well studied Escherichia coli Fis (EcFis), including an N-terminal flexible loop and a C-terminal helix-turn-helix (HTH) motif. However, the critical residues for Hin-catalyzed DNA inversion in the N-terminal loop of EcFis are not conserved in PaFis and further studies are required to investigate its exact role. A gel-electrophoresis mobility-shift assay showed that PaFis can efficiently bind to the promoter region of exsA. Structure-based mutagenesis revealed that several conserved basic residues in the HTH motif play essential roles in DNA binding. These structural and biochemical studies may help in understanding the role of PaFis in the regulation of T3SS expression and in virulence.

Indexed as

Amino Acid MotifsArginineBacterial ProteinsBinding SitesCatalytic DomainCrystallography, X-RayDimerizationDNA-Binding ProteinsEscherichia coliFactor For Inversion Stimulation ProteinGene Expression Regulation, BacterialLysineMutagenesis, Site-DirectedPhylogenyPromoter Regions, GeneticProtein BindingArginineBacterial ProteinsDNA-Binding ProteinsExsA protein, bacteriaFactor For Inversion Stimulation ProteinLysineRecombinant ProteinsTrans-ActivatorsType III Secretion SystemsVirulence Factorscrystal structureDNA-binding proteinfactor for inversion stimulationFishelix–turn–helix motifnucleoid-associated proteinPseudomonas aeruginosa

Identifiers

PMID32356522
PMCPMC7193516
OpenAlexW3023079761

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.