Evidence map›Paper›PMID 25666617›Full record

ArticleThe Journal of biological chemistry2015

A threonine stabilizes the NiC and NiR catalytic intermediates of [NiFe]-hydrogenase.

Abbas Abou-Hamdan, Pierre Ceccaldi, Hugo Lebrette, Oscar Gutiérrez-Sanz, Pierre Richaud, Laurent Cournac, Bruno Guigliarelli, Antonio L De Lacey, Christophe Léger, Anne Volbeda and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
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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 8 institutions in 2 countries.

Abbas Abou-HamdanFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France.
Pierre CeccaldiFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France.
Hugo LebretteMetalloproteins Unit, Institut de Biologie Structurale, UMR 5075 Commissariat à l'Energie Atomique/CNRS/Université Joseph Fourier, 6 rue Jules Horowitz, 38000, Grenoble, France.
Oscar Gutiérrez-SanzInstituto de Catálisis y Petroleoquímica, Consejo Superior de Investigaciones Científicas, c/Marie Curie 2, L10, 28049 Madrid, Spain.
Pierre RichaudLaboratoire de Bioénergétique et Biotechnologie des Bactéries et Microalgues, Commissariat à l'Energie Atomique, Direction des Sciences du Vivant, Institut de Biologie Environnementale et Biotechnologie, Saint-Paul-lez-Durance, F-13108, France CNRS, UMR 7265 Biologie Végétale et Microbiologie Environnementale (BVME), Saint-Paul-lez-Durance, 13108, France, and Aix-Marseille Université, BVME UMR7265, Marseille F-13284, France.
Laurent CournacLaboratoire de Bioénergétique et Biotechnologie des Bactéries et Microalgues, Commissariat à l'Energie Atomique, Direction des Sciences du Vivant, Institut de Biologie Environnementale et Biotechnologie, Saint-Paul-lez-Durance, F-13108, France CNRS, UMR 7265 Biologie Végétale et Microbiologie Environnementale (BVME), Saint-Paul-lez-Durance, 13108, France, and Aix-Marseille Université, BVME UMR7265, Marseille F-13284, France.
Bruno GuigliarelliFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France.
Antonio L De LaceyInstituto de Catálisis y Petroleoquímica, Consejo Superior de Investigaciones Científicas, c/Marie Curie 2, L10, 28049 Madrid, Spain.
Christophe LégerFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France.
Anne VolbedaMetalloproteins Unit, Institut de Biologie Structurale, UMR 5075 Commissariat à l'Energie Atomique/CNRS/Université Joseph Fourier, 6 rue Jules Horowitz, 38000, Grenoble, France.
Bénédicte BurlatFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France.
Sébastien DementinFrom the Laboratoire de Bioénergétique et Ingénierie des Protéines, Institut de Microbiologie de la Méditerranée, UMR 7281 Aix-Marseille Université/CNRS, 31 Chemin J. Aiguier, 13402 Marseille Cedex 20, France, dementin@imm.cnrs.fr.
Aix-Marseille Université · FRBioénergétique et Ingénierie des Protéines · FRCentre National de la Recherche Scientifique · FRInstitute of Environmental Biology and Biotechnology · FRConsejo Superior de Investigaciones Científicas · ESInstitut de Biologie Structurale · FRInstitut de Microbiologie de la Méditerranée · FRInstituto de Catálisis y Petroleoquímica · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The heterodimeric [NiFe] hydrogenase from Desulfovibrio fructosovorans catalyzes the reversible oxidation of H2 into protons and electrons. The catalytic intermediates have been attributed to forms of the active site (NiSI, NiR, and NiC) detected using spectroscopic methods under potentiometric but non-catalytic conditions. Here, we produced variants by replacing the conserved Thr-18 residue in the small subunit with Ser, Val, Gln, Gly, or Asp, and we analyzed the effects of these mutations on the kinetic (H2 oxidation, H2 production, and H/D exchange), spectroscopic (IR, EPR), and structural properties of the enzyme. The mutations disrupt the H-bond network in the crystals and have a strong effect on H2 oxidation and H2 production turnover rates. However, the absence of correlation between activity and rate of H/D exchange in the series of variants suggests that the alcoholic group of Thr-18 is not necessarily a proton relay. Instead, the correlation between H2 oxidation and production activity and the detection of the NiC species in reduced samples confirms that NiC is a catalytic intermediate and suggests that Thr-18 is important to stabilize the local protein structure of the active site ensuring fast NiSI-NiC-NiR interconversions during H2 oxidation/production.

Indexed as

Amino Acid SequenceAmino Acid SubstitutionBacterial ProteinsBiocatalysisCatalytic DomainCrystallography, X-RayDesulfovibrioEnzyme StabilityHydrogenaseHydrogen BondingKineticsModels, MolecularOxidation-ReductionThreonineBacterial ProteinsHydrogenasenickel-iron hydrogenaseThreonineElectron Paramagnetic Resonance (EPR)Enzyme KineticsFourier Transform IR (FTIR)HydrogenaseX-ray Crystallography

Identifiers

PMID25666617
PMCPMC4375504
OpenAlexW2161226840

What OpenQuestion holds

Textmetadata
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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.