Evidence map›Paper›PMID 22837698›Full record

ArticleInternational journal of molecular sciences2012

Solution NMR structure of hypothetical protein CV_2116 encoded by a viral prophage element in Chromobacterium violaceum.

Yunhuang Yang, Theresa A Ramelot, John R Cort, Maite Garcia, Adelinda Yee, Cheryl H Arrowsmith, Michael A Kennedy

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 34% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 5 institutions in 2 countries.

Yunhuang YangDepartment of Chemistry and Biochemistry and the Northeast Structural Genomics Consortium, Miami University, Oxford, OH 45056, USA.
Theresa A RamelotDepartment of Chemistry and Biochemistry and the Northeast Structural Genomics Consortium, Miami University, Oxford, OH 45056, USA.
John R CortBiological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
Maite GarciaCampbell Family Cancer Research Institute, Ontario Cancer Institute and the Northeast Structural Genomics Consortium, University Health Network, Toronto, ON, M5G 2C4, Canada.
Adelinda YeeCampbell Family Cancer Research Institute, Ontario Cancer Institute and the Northeast Structural Genomics Consortium, University Health Network, Toronto, ON, M5G 2C4, Canada.
Cheryl H ArrowsmithCampbell Family Cancer Research Institute, Ontario Cancer Institute and the Northeast Structural Genomics Consortium, University Health Network, Toronto, ON, M5G 2C4, Canada.
Michael A KennedyDepartment of Chemistry and Biochemistry and the Northeast Structural Genomics Consortium, Miami University, Oxford, OH 45056, USA.
Miami University · USOntario Institute for Cancer Research · CAPacific Northwest National Laboratory · USStructural Genomics Consortium · CAUniversity Health Network · CA

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
NIGMS NIH HHS U54 GM074958NIGMS NIH HHS U54-GM074958NIGMS NIH HHS U54 GM094597NIGMS NIH HHS U54-GM094597
6 · The paper itself

Abstract

CV_2116 is a small hypothetical protein of 82 amino acids from the Gram-negative coccobacillus Chromobacterium violaceum. A PSI-BLAST search using the CV_2116 sequence as a query identified only one hit (E = 2e(-07)) corresponding to a hypothetical protein OR16_04617 from Cupriavidus basilensis OR16, which failed to provide insight into the function of CV_2116. The CV_2116 gene was cloned into the p15TvLic expression plasmid, transformed into E. coli, and (13)C- and (15)N-labeled NMR samples of CV_2116 were overexpressed in E. coli and purified for structure determination using NMR spectroscopy. The resulting high-quality solution NMR structure of CV_2116 revealed a novel α + β fold containing two anti-parallel β-sheets in the N-terminal two-thirds of the protein and one α-helix in the C-terminal third of the protein. CV_2116 does not belong to any known protein sequence family and a Dali search indicated that no similar structures exist in the protein data bank. Although no function of CV_2116 could be derived from either sequence or structural similarity searches, the neighboring genes of CV_2116 encode various proteins annotated as similar to bacteriophage tail assembly proteins. Interestingly, C. violaceum exhibits an extensive network of bacteriophage tail-like structures that likely result from lateral gene transfer by incorporation of viral DNA into its genome (prophages) due to bacteriophage infection. Indeed, C. violaceum has been shown to contain four prophage elements and CV_2116 resides in the fourth of these elements. Analysis of the putative operon in which CV_2116 resides indicates that CV_2116 might be a component of the bacteriophage tail-like assembly that occurs in C. violaceum.

Indexed as

ChromobacteriumDatabases, ProteinNuclear Magnetic Resonance, BiomolecularProphagesProtein Structure, SecondaryProtein Structure, TertiaryViral ProteinsViral Proteinsbacteriophage tail assemblyChromobacterium violaceumCV_2116lateral gene transferNMRprophagesolution structurestructural genomics

Identifiers

PMID22837698
PMCPMC3397530
OpenAlexW2032276570

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.