Evidence map›Paper›PMID 31076553›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Switch-like activation of Bruton's tyrosine kinase by membrane-mediated dimerization.

Jean K Chung, Laura M Nocka, Aubrianna Decker, Qi Wang, Theresa A Kadlecek, Arthur Weiss, John Kuriyan, Jay T Groves

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 63 citations in OpenAlex.

  1. LAT condensation gates PLCγ1 activation via bimodal LAT phosphorylation.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  3. Two-step mechanism of Bruton's tyrosine kinase membrane recruitment and activation.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

8 authors at 3 institutions in 1 country.

Jean K ChungDepartment of Chemistry, University of California, Berkeley, CA 94720.
Laura M NockaDepartment of Chemistry, University of California, Berkeley, CA 94720.
Aubrianna DeckerDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720.
Qi WangDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720.
Theresa A KadlecekDepartment of Microbiology and Immunology, University of California, San Francisco, CA 94143.
Arthur WeissDepartment of Microbiology and Immunology, University of California, San Francisco, CA 94143.
John KuriyanDepartment of Chemistry, University of California, Berkeley, CA 94720; kuriyan@berkeley.edu jtgroves@lbl.gov.
Jay T GrovesDepartment of Chemistry, University of California, Berkeley, CA 94720; kuriyan@berkeley.edu jtgroves@lbl.gov.
University of California, Berkeley · USHoward Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Understand the metabolic fitness of naïve T cellsP01AI091580 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI JEROEN ROOSE · 2011 to 2026
$31.1M
MOLECULAR BIOPHYSICS TRAINING GRANTT32GM008295 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HURLEY, JAMES H, WEMMER, DAVID E · 1989 to 2022
$8.1M
ECM geometrical and mechanical properties modulate RTK signalingU01CA202241 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI GROVES, JAY T., WEAVER, VALERIE MARIE · 2015 to 2019
$3.3M
NCI NIH HHS U01 CA202241NIAID NIH HHS P01 AI091580NIGMS NIH HHS T32 GM008295
6 · The paper itself

Abstract

The transformation of molecular binding events into cellular decisions is the basis of most biological signal transduction. A fundamental challenge faced by these systems is that reliance on protein-ligand chemical affinities alone generally results in poor sensitivity to ligand concentration, endangering the system to error. Here, we examine the lipid-binding pleckstrin homology and Tec homology (PH-TH) module of Bruton's tyrosine kinase (Btk). Using fluorescence correlation spectroscopy (FCS) and membrane-binding kinetic measurements, we identify a phosphatidylinositol (3-5)-trisphosphate (PIP

Indexed as

Agammaglobulinaemia Tyrosine KinaseAnimalsB-LymphocytesCell LineChickensMiceModels, MolecularMutationPhosphatidylinositol PhosphatesPhosphorylationProtein ConformationProtein DomainsProtein MultimerizationSignal TransductionAgammaglobulinaemia Tyrosine KinaseBtk protein, mousePhosphatidylinositol PhosphatesBruton’s tyrosine kinasePIP3signalingultrasensitivity

Identifiers

PMID31076553
PMCPMC6561188
OpenAlexW2952113952

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.