Evidence map›Paper›PMID 19130299›Full record

ArticleJournal of structural and functional genomics2009

The Center for Eukaryotic Structural Genomics.

John L Markley, David J Aceti, Craig A Bingman, Brian G Fox, Ronnie O Frederick, Shin-ichi Makino, Karl W Nichols, George N Phillips, John G Primm, Sarata C Sahu and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of structural and functional genomics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Development of a cell-free protein synthesis system for practical use.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2021
    Article
  5. Structural Features of Tight-Junction Proteins.International journal of molecular sciences · 2019
    Review
  6. Biomolecular NMR: Past and future.Archives of biochemistry and biophysics · 2017
    Article
  7. Databases, Repositories, and Other Data Resources in Structural Biology.Methods in molecular biology (Clifton, N.J.) · 2017
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. First experiences with semi-autonomous robotic harvesting of protein crystals.Journal of structural and functional genomics · 2011
    Article
  16. Article
  17. Article
  18. Review
  19. Mechanisms of organelle division and inheritance and their implications regarding the origin of eukaryotic cells.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2010
    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

14 authors at 2 institutions in 1 country.

John L MarkleyCenter for Eukaryotic Structural Genomics, Biochemistry Department, University of Wisconsin-Madison, Madison, WI 53706, USA. markley@nmrfam.wisc.edu
David J Aceti
Craig A Bingman
Brian G Fox
Ronnie O Frederick
Shin-ichi Makino
Karl W Nichols
George N Phillips
John G Primm
Sarata C Sahu
Frank C Vojtik
Brian F Volkman
Russell L Wrobel
Zsolt Zolnai
University of Wisconsin–Madison · USMedical College of Wisconsin · US

Funding

Specialized Center for Eukaryotic Structural GenomicsU54GM074901 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI MARKLEY, JOHN LUTE · 2005 to 2009
$18.9M
WATER DISTRIB:PHYSICAL PROPERT:PIZZA &LMPS MOZZARELLA CHEESES:EARLY STAGE MATURP41RR002301 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI MARKLEY, JOHN LUTE · 1985 to 2011
$13.0M
900 MHz NMR Spectrometer Biomolecular InvestigationsP41GM066326 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI MARKLEY, JOHN L · 2002 to 2006
$5.0M
NCRR NIH HHS P41 RR002301NCRR NIH HHS P41 RR02301NIGMS NIH HHS P41 GM066326NIGMS NIH HHS P41 GM66326NIGMS NIH HHS U54 GM074901
6 · The paper itself

Abstract

The Center for Eukaryotic Structural Genomics (CESG) is a "specialized" or "technology development" center supported by the Protein Structure Initiative (PSI). CESG's mission is to develop improved methods for the high-throughput solution of structures from eukaryotic proteins, with a very strong weighting toward human proteins of biomedical relevance. During the first three years of PSI-2, CESG selected targets representing 601 proteins from Homo sapiens, 33 from mouse, 10 from rat, 139 from Galdieria sulphuraria, 35 from Arabidopsis thaliana, 96 from Cyanidioschyzon merolae, 80 from Plasmodium falciparum, 24 from yeast, and about 25 from other eukaryotes. Notably, 30% of all structures of human proteins solved by the PSI Centers were determined at CESG. Whereas eukaryotic proteins generally are considered to be much more challenging targets than prokaryotic proteins, the technology now in place at CESG yields success rates that are comparable to those of the large production centers that work primarily on prokaryotic proteins. We describe here the technological innovations that underlie CESG's platforms for bioinformatics and laboratory information management, target selection, protein production, and structure determination by X-ray crystallography or NMR spectroscopy.

Indexed as

AnimalsCrystallography, X-RayGenomicsHumansMulti-Institutional SystemsNuclear Magnetic Resonance, BiomolecularProtein ConformationProteinsProteomicsProteins

Identifiers

PMID19130299
PMCPMC2705709
OpenAlexW1987250670

What OpenQuestion holds

Textmetadata
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.