Evidence map›Paper›PMID 19091303›Full record

ReviewCellular signalling2009

Protein scaffolds in MAP kinase signalling.

Matthew D Brown, David B Sacks

Abstract readReview
In one paragraph

Review in Cellular signalling, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
–field-weighted citation impact
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

126 citing papers in PubMed.

  1. Article
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  16. Article
  17. Short Arrestin-3-Derived Peptides Activate JNK3 in Cells.International journal of molecular sciences · 2022
    Article
  18. Scaffolding of Mitogen-Activated Protein Kinase Signaling by β-Arrestins.International journal of molecular sciences · 2022
    Review
  19. Review
  20. Review

66 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

2 authors.

Matthew D BrownDepartment of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, United States.
David B Sacks

Funding

CALMODULIN IN NEOPLASTIC TRANSFORMATION OF BREAST TISSUER01CA075205 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKS, DAVID B · 1999 to 2008
$2.8M
NCI NIH HHS R01 CA075205
6 · The paper itself

Abstract

The mitogen-activated protein kinase (MAPK) pathway allows cells to interpret external signals and respond in an appropriate way. Diverse cellular functions, ranging from differentiation and proliferation to migration and inflammation, are regulated by MAPK signalling. Therefore, cells have developed mechanisms by which this single pathway modulates numerous cellular responses from a wide range of activating factors. This specificity is achieved by several mechanisms, including temporal and spatial control of MAPK signalling components. Key to this control are protein scaffolds, which are multidomain proteins that interact with components of the MAPK cascade in order to assemble signalling complexes. Studies conducted on different scaffolds, in different biological systems, have shown that scaffolds exert substantial control over MAPK signalling, influencing the signal intensity, time course and, importantly, the cellular responses. Protein scaffolds, therefore, are integral elements to the modulation of the MAPK network in fundamental physiological processes.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsArrestinsbeta-ArrestinsCell CompartmentationDrug Delivery SystemsExtracellular Signal-Regulated MAP KinasesHumansMAP Kinase Kinase 4MAP Kinase Kinase KinasesMAP Kinase Signaling SystemMultiprotein Complexesp38 Mitogen-Activated Protein KinasesProtein Kinasesras GTPase-Activating ProteinsReceptors, InterleukinAdaptor Proteins, Signal TransducingArrestinsbeta-ArrestinsExtracellular Signal-Regulated MAP KinasesIL17RD protein, humanIQ motif containing GTPase activating protein 1KSR-1 protein kinaseLAMTOR3 protein, humanMAP Kinase Kinase 4MAP Kinase Kinase KinasesMultiprotein Complexesp38 Mitogen-Activated Protein KinasesProtein Kinasesras GTPase-Activating ProteinsReceptors, Interleukin

Identifiers

PMID19091303
PMCPMC2668224

What OpenQuestion holds

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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.