Evidence map›Paper›PMID 29630677›Full record

ArticlePloS one2018

The crystal structure of XdpB, the bacterial old yellow enzyme, in an FMN-free form.

Jiří Zahradník, Petr Kolenko, Andrea Palyzová, Jiří Černý, Lucie Kolářová, Eva Kyslíková, Helena Marešová, Michal Grulich, Jaroslav Nunvar, Miroslav Šulc and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. 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
0.4field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

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

12 authors at 3 institutions in 1 country.

Jiří ZahradníkInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.
Petr KolenkoInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.
Andrea PalyzováInstitute of Microbiology CAS, v. v. i., Prague, Czech Republic.
Jiří ČernýInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.
Lucie KolářováInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.
Eva KyslíkováInstitute of Microbiology CAS, v. v. i., Prague, Czech Republic.
Helena MarešováInstitute of Microbiology CAS, v. v. i., Prague, Czech Republic.
Michal GrulichInstitute of Microbiology CAS, v. v. i., Prague, Czech Republic.
Jaroslav NunvarInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.
Miroslav ŠulcDepartment of Biochemistry, Faculty of Science, Charles University Prague, Czech Republic.
Pavel KyslíkInstitute of Microbiology CAS, v. v. i., Prague, Czech Republic.
Bohdan SchneiderInstitute of Biotechnology CAS, v. v. i., BIOCEV, Vestec, Prague West, Czech Republic.ORCID 0000-0001-7855-3690
Czech Academy of Sciences, Institute of Biotechnology · CZCzech Academy of Sciences, Institute of Microbiology · CZCharles University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Old Yellow Enzymes (OYEs) are NAD(P)H dehydrogenases of not fully resolved physiological roles that are widespread among bacteria, plants, and fungi and have a great potential for biotechnological applications. We determined the apo form crystal structure of a member of the OYE class, glycerol trinitrate reductase XdpB, from Agrobacterium bohemicum R89-1 at 2.1 Å resolution. In agreement with the structures of the related bacterial OYEs, the structure revealed the TIM barrel fold with an N-terminal β-hairpin lid, but surprisingly, the structure did not contain its cofactor FMN. Its putative binding site was occupied by a pentapeptide TTSDN from the C-terminus of a symmetry related molecule. Biochemical experiments confirmed a specific concentration-dependent oligomerization and a low FMN content. The blocking of the FMN binding site can exist in vivo and regulates enzyme activity. Our bioinformatic analysis indicated that a similar self-inhibition could be expected in more OYEs which we designated as subgroup OYE C1. This subgroup is widespread among G-bacteria and can be recognized by the conserved sequence GxxDYP in proximity of the C termini. In proteobacteria, the C1 subgroup OYEs are typically coded in one operon with short-chain dehydrogenase. This operon is controlled by the tetR-like transcriptional regulator. OYEs coded in these operons are unlikely to be involved in the oxidative stress response as the other known members of the OYE family because no upregulation of XdpB was observed after exposing A. bohemicum R89-1 to oxidative stress.

Indexed as

AgrobacteriumBacterial ProteinsCatalytic DomainComputational BiologyCrystallography, X-RayFlavin MononucleotideGenes, BacterialKineticsModels, MolecularNADPH DehydrogenaseOperonOxidative StressOxidoreductasesProtein Structure, QuaternaryBacterial ProteinsFlavin Mononucleotideglyceryl trinitrate reductaseNADPH DehydrogenaseOxidoreductases

Identifiers

PMID29630677
PMCPMC5891007
OpenAlexW2796570521

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.