Evidence map›Paper›PMID 19132843›Full record

ArticleBiochemistry2009

Role of histidine-86 in the catalytic mechanism of ferredoxin:thioredoxin reductase.

Elizabeth M Walters, Ricardo Garcia-Serres, Sunil G Naik, Florence Bourquin, Dominique A Glauser, Peter Schürmann, Boi Hanh Huynh, Michael K Johnson

Open access · greenAbstract readComparative Study
In one paragraph

Article in Biochemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Elizabeth M WaltersDepartment of Chemistry and Center for Metalloenzyme Studies, University of Georgia, Athens, Georgia 30602, USA.
Ricardo Garcia-Serres
Sunil G Naik
Florence Bourquin
Dominique A Glauser
Peter Schürmann
Boi Hanh Huynh
Michael K Johnson
Emory University · USUniversity of Neuchâtel · CHUniversity of Georgia · US

Funding

Assembly of Biological Iron-Sulfur ClustersR01GM062524 · NIGMS · UNIVERSITY OF GEORGIA (UGA) · PI JOHNSON, MICHAEL K. · 2001 to 2012
$2.7M
OXYGEN ACTIVATION BY NON HEME FE PROTEINSR01GM047295 · NIGMS · EMORY UNIVERSITY · PI HUYNH, BOI-HANH V. · 1992 to 2008
$1.7M
SIGNALING PATHWAYS THAT REGULATE MITOSISR01GM062542 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI GUADAGNO, THOMAS M · 2001 to 2005
$1.2M
NIGMS NIH HHS GM47295NIGMS NIH HHS GM62542NIGMS NIH HHS R01 GM047295NIGMS NIH HHS R01 GM062524NIGMS NIH HHS R01 GM062542
6 · The paper itself

Abstract

Ferredoxin:thioredoxin reductase catalyzes the reduction of thioredoxins in plant chloroplasts using the [Fe2S2] ferredoxin as a one-electron donor and as such plays a central role in light regulation of oxygenic photosynthesis. The active-site comprises a [Fe4S4] cluster next to a redox-active disulfide that is cleaved in sequential one-electron steps and the combination of spectroscopic and crystallographic studies have revealed a catalytic mechanism involving novel site specific cluster chemistry in the oxidized, one-electron- and two-electron-reduced redox states. Histidine-86 has emerged as a potential proton donor/acceptor in the catalytic mechanism based on redox-related changes in the positioning of the imidazole ring during redox cycling and greatly decreased activity for the H86Y variant. Here we report on spectroscopic and redox characterization of the [Fe4S4] center in Synechocystis sp. PCC 6803 H86Y ferredoxin:thoredoxin reductase in the accessible redox states of both the as purified and N-ethylmaleimide-modified forms, using the combination of UV-visible absorption and variable-temperature magnetic circular dichroism, EPR, resonance Raman and Mössbauer spectroscopies. The results demonstrate that His86 is required for formation of the partially valence-localized [Fe4S4]2+ cluster that is the hallmark of two-electron-reduced intermediate. Taken together with the available structural data, the spectroscopic results indicate a functional role for His86 in protonation/deprotonation of the cluster-interacting thiol and anchoring the cluster interacting thiol in close proximity to the cluster in the two-electron-reduced intermediate.

Indexed as

Bacterial ProteinsCatalysisElectronsFerredoxinsHistidineIron-Sulfur ProteinsOxidation-ReductionProtonsSulfhydryl CompoundsSynechocystisThioredoxin-Disulfide ReductaseBacterial ProteinsFerredoxinsHistidineIron-Sulfur ProteinsProtonsSulfhydryl CompoundsThioredoxin-Disulfide Reductase

Identifiers

PMID19132843
PMCPMC2709840
OpenAlexW2093160369

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.