Evidence map›Paper›PMID 24039739›Full record

ArticlePloS one2013

Structure determination and biochemical characterization of a putative HNH endonuclease from Geobacter metallireducens GS-15.

Shuang-yong Xu, Alexandre P Kuzin, Jayaraman Seetharaman, Alice Gutjahr, Siu-Hong Chan, Yang Chen, Rong Xiao, Thomas B Acton, Gaetano T Montelione, Liang Tong

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. 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
2.6field-weighted citation impact, top 11% 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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  9. Staphylococcal pathogenicity island DNA packaging system involving cos-site packaging and phage-encoded HNH endonucleases.Proceedings of the National Academy of Sciences of the United States of America · 2014
    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

10 authors at 4 institutions in 1 country.

Shuang-yong XuNew England Biolabs, Inc. Research Department, Ipswich, Massachusetts, United States of America.
Alexandre P Kuzin
Jayaraman Seetharaman
Alice Gutjahr
Siu-Hong Chan
Yang Chen
Rong Xiao
Thomas B Acton
Gaetano T Montelione
Liang Tong
Columbia University · USNew England Biolabs (United States) · USRutgers, The State University of New Jersey · USNew York Structural Biology Center · US

Funding

Sub-project 9U54GM074958 · NIGMS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI KENNEDY, MICHAEL ALLEN · 2005 to 2009
$56.6M
University of Georgia ProjectU54GM094597 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI ROST, BURKHARD · 2010 to 2014
$36.9M
Y-FAMILY POLYMERASES AND CO-FACTORS IN TRANSLESION REPLICATIONP41RR015301 · NCRR · CORNELL UNIVERSITY ITHACA · PI EISENBERG, DAVID · 2001 to 2011
$28.2M
NCRR NIH HHS P41 RR015301NIGMS NIH HHS U54 GM074958NIGMS NIH HHS U54 GM094597
6 · The paper itself

Abstract

The crystal structure of a putative HNH endonuclease, Gmet_0936 protein from Geobacter metallireducens GS-15, has been determined at 2.6 Å resolution using single-wavelength anomalous dispersion method. The structure contains a two-stranded anti-parallel β-sheet that are surrounded by two helices on each face, and reveals a Zn ion bound in each monomer, coordinated by residues Cys38, Cys41, Cys73, and Cys76, which likely plays an important structural role in stabilizing the overall conformation. Structural homologs of Gmet_0936 include Hpy99I endonuclease, phage T4 endonuclease VII, and other HNH endonucleases, with these enzymes sharing 15-20% amino acid sequence identity. An overlay of Gmet_0936 and Hpy99I structures shows that most of the secondary structure elements, catalytic residues as well as the zinc binding site (zinc ribbon) are conserved. However, Gmet_0936 lacks the N-terminal domain of Hpy99I, which mediates DNA binding as well as dimerization. Purified Gmet_0936 forms dimers in solution and a dimer of the protein is observed in the crystal, but with a different mode of dimerization as compared to Hpy99I. Gmet_0936 and its N77H variant show a weak DNA binding activity in a DNA mobility shift assay and a weak Mn²⁺-dependent nicking activity on supercoiled plasmids in low pH buffers. The preferred substrate appears to be acid and heat-treated DNA with AP sites, suggesting Gmet_0936 may be a DNA repair enzyme.

Indexed as

Amino Acid SequenceAmino Acid SubstitutionBacterial ProteinsCatalytic DomainCrystallography, X-RayDNA-(Apurinic or Apyrimidinic Site) LyaseDNA CleavageDNA Repair EnzymesGeobacterHydrogen-Ion ConcentrationModels, MolecularMolecular Sequence DataMutagenesis, Site-DirectedPolydeoxyribonucleotidesProtein BindingProtein Structure, QuaternaryBacterial ProteinsDNA-(Apurinic or Apyrimidinic Site) LyaseDNA Repair EnzymesPolydeoxyribonucleotides

Identifiers

PMID24039739
PMCPMC3765158
OpenAlexW2103468693

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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.