Evidence map›Paper›PMID 23349695›Full record

ArticlePloS one2013

Integron gene cassettes: a repository of novel protein folds with distinct interaction sites.

Visaahini Sureshan, Chandrika N Deshpande, Yan Boucher, Jeremy E Koenig, Midwest Center for Structural Genomics, H W Stokes, Stephen J Harrop, Paul M G Curmi, Bridget C Mabbutt

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.9field-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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Integrons: past, present, and future.Microbiology and molecular biology reviews : MMBR · 2014
    Review
  5. Review
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

9 authors at 5 institutions in 2 countries.

Visaahini SureshanDepartment of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, New South Wales, Australia.
Chandrika N Deshpande
Yan Boucher
Jeremy E Koenig
Midwest Center for Structural Genomics
H W Stokes
Stephen J Harrop
Paul M G Curmi
Bridget C Mabbutt
Macquarie University · AUUNSW Sydney · AUDalhousie University · CAUniversity of Alberta · CAUniversity of Technology Sydney · AU

Funding

The Midwest Center for Structural GenomicsU54GM074942 · NIGMS · UNIVERSITY OF CHICAGO · PI FREMONT, DAVED H. · 2005 to 2009
$51.0M
Midwest Center for Structural GenomicsU54GM094585 · NIGMS · UNIVERSITY OF CHICAGO · PI MINOR, WLADEK · 2010 to 2014
$33.7M
Structures of Mtb proteins conferring susceptibility to known Mtb inhibitorsU01GM094568 · NIGMS · TEXAS A&M UNIVERSITY · PI SACCHETTINI, JAMES C · 2010 to 2014
$6.0M
NIGMS NIH HHS GM074942NIGMS NIH HHS GM094568NIGMS NIH HHS U01 GM094568NIGMS NIH HHS U54 GM074942NIGMS NIH HHS U54 GM094585
6 · The paper itself

Abstract

Mobile gene cassettes captured within integron arrays encompass a vast and diverse pool of genetic novelty. In most cases, functional annotation of gene cassettes directly recovered by cassette-PCR is obscured by their characteristically high sequence novelty. This inhibits identification of those specific functions or biological features that might constitute preferential factors for lateral gene transfer via the integron system. A structural genomics approach incorporating x-ray crystallography has been utilised on a selection of cassettes to investigate evolutionary relationships hidden at the sequence level. Gene cassettes were accessed from marine sediments (pristine and contaminated sites), as well as a range of Vibrio spp. We present six crystal structures, a remarkably high proportion of our survey of soluble proteins, which were found to possess novel folds. These entirely new structures are diverse, encompassing all-α, α+β and α/β fold classes, and many contain clear binding pocket features for small molecule substrates. The new structures emphasise the large repertoire of protein families encoded within the integron cassette metagenome and which remain to be characterised. Oligomeric association is a notable recurring property common to these new integron-derived proteins. In some cases, the protein-protein contact sites utilised in homomeric assembly could instead form suitable contact points for heterogeneous regulator/activator proteins or domains. Such functional features are ideal for a flexible molecular componentry needed to ensure responsive and adaptive bacterial functions.

Indexed as

Amino Acid SequenceBacterial ProteinsBinding SitesCrystallography, X-RayGenes, BacterialGene Transfer, HorizontalIntegronsMetagenomeModels, MolecularMolecular Sequence DataOligonucleotide Array Sequence AnalysisProtein BindingProtein Structure, SecondaryVibrio choleraeBacterial Proteins

Identifiers

PMID23349695
PMCPMC3548836
OpenAlexW1999426918

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.