Evidence map›Paper›PMID 27909043›Full record

ArticleMolecular systems biology2016

An atlas of human kinase regulation.

David Ochoa, Mindaugas Jonikas, Robert T Lawrence, Bachir El Debs, Joel Selkrig, Athanasios Typas, Judit Villén, Silvia Dm Santos, Pedro Beltrao

Abstract read
In one paragraph

Article in Molecular systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 1 pooled it
–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

68 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  17. Journal of proteome research · 2023
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8 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.

David OchoaEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK.
Mindaugas JonikasQuantitative Cell Biology Group, MRC Clinical Sciences Centre, Imperial College, London, UK.
Robert T LawrenceDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Bachir El DebsGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Joel SelkrigGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Athanasios TypasGenome Biology Unit, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Judit VillénDepartment of Genome Sciences, University of Washington, Seattle, WA, USA.
Silvia Dm SantosQuantitative Cell Biology Group, MRC Clinical Sciences Centre, Imperial College, London, UK.
Pedro BeltraoEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, UK pbeltrao@ebi.ac.uk.ORCID http://orcid.org/0000-0002-2724-7703

Funding

Towards a comprehensive roadmap of cellular signaling.R35GM119536 · NIGMS · UNIVERSITY OF WASHINGTON · PI VILLEN, JUDIT · 2016 to 2020
$2.2M
Proteome-wide study of signaling networks in cancer by mass spectrometryR00CA140789 · NCI · UNIVERSITY OF WASHINGTON · PI VILLEN, JUDIT · 2010 to 2012
$732k
Proteome-wide study of signaling networks in cancer by mass spectrometryK99CA140789 · NCI · HARVARD MEDICAL SCHOOL · PI VILLEN, JUDIT · 2009 to 2009
$135k
Medical Research Council MC_UP_1102/9NCI NIH HHS K99 CA140789NCI NIH HHS R00 CA140789NIGMS NIH HHS R35 GM119536
6 · The paper itself

Abstract

The coordinated regulation of protein kinases is a rapid mechanism that integrates diverse cues and swiftly determines appropriate cellular responses. However, our understanding of cellular decision-making has been limited by the small number of simultaneously monitored phospho-regulatory events. Here, we have estimated changes in activity in 215 human kinases in 399 conditions derived from a large compilation of phosphopeptide quantifications. This atlas identifies commonly regulated kinases as those that are central in the signaling network and defines the logic relationships between kinase pairs. Co-regulation along the conditions predicts kinase-complex and kinase-substrate associations. Additionally, the kinase regulation profile acts as a molecular fingerprint to identify related and opposing signaling states. Using this atlas, we identified essential mediators of stem cell differentiation, modulators of Salmonella infection, and new targets of AKT1. This provides a global view of human phosphorylation-based signaling and the necessary context to better understand kinase-driven decision-making.

Indexed as

Cell DifferentiationDatabases, ProteinGene Expression Regulation, EnzymologicHeLa CellsHuman Embryonic Stem CellsHumansPhosphorylationProtein KinasesProteomicsSignal TransductionSystems BiologyProtein Kinasescell fatehumankinase activityphosphoproteomicssignaling

Identifiers

PMID27909043
PMCPMC5199121

What OpenQuestion holds

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LicenceCC BY
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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.