Evidence map›Paper›PMID 15302935›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2004

Large-scale characterization of HeLa cell nuclear phosphoproteins.

Sean A Beausoleil, Mark Jedrychowski, Daniel Schwartz, Joshua E Elias, Judit Villén, Jiaxu Li, Martin A Cohn, Lewis C Cantley, Steven P Gygi

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 523 papers.

0numbers the graph read from it
0cells of the map it votes in
523citing papers in PubMed
36.1field-weighted citation impact, top 1% 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

523 citing papers in PubMed, 1,385 citations in OpenAlex.

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  10. bioRxiv : the preprint server for biology · 2024
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  17. Demystifying PTM Identification Using MODplus: Best Practices and Pitfalls.Methods in molecular biology (Clifton, N.J.) · 2024
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463 more citing papers are in PubMed but not listed here.

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 4 institutions in 3 countries.

Sean A BeausoleilDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Mark Jedrychowski
Daniel Schwartz
Joshua E Elias
Judit Villén
Jiaxu Li
Martin A Cohn
Lewis C Cantley
Steven P Gygi
Harvard University · USDana-Farber Cancer Institute · USBeth Israel Deaconess Medical Center · USInstitute of Cell Biology · UA

Funding

New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
PROTEIN KINASE SIGNALING PATHWAYSR01GM056203 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CANTLEY, LEWIS C. · 1997 to 2012
$4.5M
TECHNOLOGY FOR AUTOMATED ANALYSIS OF PROTEOMESK22HG000041 · NHGRI · UNIVERSITY OF WASHINGTON · PI GYGI, STEVEN P · 2000 to 2004
$1.2M
INSTITUTIONAL TRAINING GRANT IN GENOMIC SCIENCET32HG000041 · NHGRI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SMITH, TEMPLE F · 1995 to 1999
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NHGRI NIH HHS HG00041NHGRI NIH HHS K22 HG000041NHGRI NIH HHS T32 HG000041NIGMS NIH HHS GM67945NIGMS NIH HHS GMS6203NIGMS NIH HHS R01 GM056203NIGMS NIH HHS R01 GM067945
6 · The paper itself

Abstract

Determining the site of a regulatory phosphorylation event is often essential for elucidating specific kinase-substrate relationships, providing a handle for understanding essential signaling pathways and ultimately allowing insights into numerous disease pathologies. Despite intense research efforts to elucidate mechanisms of protein phosphorylation regulation, efficient, large-scale identification and characterization of phosphorylation sites remains an unsolved problem. In this report we describe an application of existing technology for the isolation and identification of phosphorylation sites. By using a strategy based on strong cation exchange chromatography, phosphopeptides were enriched from the nuclear fraction of HeLa cell lysate. From 967 proteins, 2,002 phosphorylation sites were determined by tandem MS. This unprecedented large collection of sites permitted a detailed accounting of known and unknown kinase motifs and substrates.

Indexed as

Amino Acid SequenceBinding SitesCell NucleusChromatography, Ion ExchangeComputational BiologyHeLa CellsHumansMass SpectrometryMolecular Sequence DataNuclear ProteinsPhosphoproteinsPhosphorylationSerineThreonineTrypsinNuclear ProteinsPhosphoproteinsSerineThreonineTrypsin

Identifiers

PMID15302935
PMCPMC514446
OpenAlexW2129777487

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.