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Author Details
Full Name
Jack Taunton
Affiliation
University of California san francisco
ORCID
Career Start Year
1996
Papers
102
H Index
53
Expertise
CM4AI Collaborator
Trey Ideker (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36638793
An E3 ligase network engages GCN1 to promote the degradation of translation factors on stalled ribosomes.
Cell
2023
37460812
Direct mapping of ligandable tyrosines and lysines in cells with chiral sulfonyl fluoride probes.
Nat Chem
2023
37354015
Large library docking for novel SARS-CoV-2 main protease non-covalent and covalent inhibitors.
Protein Sci
2023
37020024
mRNA decoding in human is kinetically and structurally distinct from bacteria.
Nature
2023
37169961
Signal peptide mimicry primes Sec61 for client-selective inhibition.
Nat Chem Biol
2023
36123449
Synthesis and single-molecule imaging reveal stereospecific enhancement of binding kinetics by the antitumour eEF1A antagonist SR-A3.
Nat Chem
2022
35434798
Inhibition of the Sec61 translocon overcomes cytokine-induced glucocorticoid resistance in T-cell acute lymphoblastic leukaemia.
Br J Haematol
2022
35590003
Reversible lysine-targeted probes reveal residence time-based kinase selectivity.
Nat Chem Biol
2022
36480603
IFITM proteins assist cellular uptake of diverse linked chemotypes.
Science
2022
36264623
Didemnin B and ternatin-4 differentially inhibit conformational changes in eEF1A required for aminoacyl-tRNA accommodation into mammalian ribosomes.
Elife
2022
34251165
Identifying the Cellular Target of Cordyheptapeptide A and Synthetic Derivatives.
ACS Chem Biol
2021
33681312
Corrigendum: p90RSK-MAGI1 Module Controls Endothelial Permeability by Post-translational Modifications of MAGI1 and Hippo Pathway.
Front Cardiovasc Med
2021
32353859
A SARS-CoV-2 protein interaction map reveals targets for drug repurposing.
Nature
2020
32105459
Discovery of Lysine-Targeted eIF4E Inhibitors through Covalent Docking.
J Am Chem Soc
2020
32009391
Ligand Conformational Bias Drives Enantioselective Modification of a Surface-Exposed Lysine on Hsp90.
J Am Chem Soc
2020
33304925
p90RSK-MAGI1 Module Controls Endothelial Permeability by Post-translational Modifications of MAGI1 and Hippo Pathway.
Front Cardiovasc Med
2020
32589729
CRISPR-based screens uncover determinants of immunotherapy response in multiple myeloma.
Blood Adv
2020
30586719
Senescent Phenotype Induced by p90RSK-NRF2 Signaling Sensitizes Monocytes and Macrophages to Oxidative Stress in HIV-Positive Individuals.
Circulation
2019
31045573
Endothelial senescence is induced by phosphorylation and nuclear export of telomeric repeat binding factor 2-interacting protein.
JCI Insight
2019
30944250
MAGI1 as a link between endothelial activation and ER stress drives atherosclerosis.
JCI Insight
2019
30633551
Lysine-Targeted Inhibitors and Chemoproteomic Probes.
Annu Rev Biochem
2019
29622655
Repurposing tofacitinib as an anti-myeloma therapeutic to reverse growth-promoting effects of the bone marrow microenvironment.
Haematologica
2018
29540678
Inhibition of Sec61-dependent translocation by mycolactone uncouples the integrated stress response from ER stress, driving cytotoxicity via translational activation of ATF4.
Cell Death Dis
2018
28051857
Broad-Spectrum Kinase Profiling in Live Cells with Lysine-Targeted Sulfonyl Fluoride Probes.
J Am Chem Soc
2017
28484265
JAK/STAT pathway inhibition overcomes IL7-induced glucocorticoid resistance in a subset of human T-cell acute lymphoblastic leukemias.
Leukemia
2017
29259099
IL-2Rβ abundance differentially tunes IL-2 signaling dynamics in CD4<sup>+</sup> and CD8<sup>+</sup> T cells.
Sci Signal
2017
29054929
Mitogen- and stress-activated protein kinase 1 is required for gonadotropin-releasing hormone-mediated activation of gonadotropin α-subunit expression.
J Biol Chem
2017
29296813
Oncogenic role and therapeutic targeting of ABL-class and JAK-STAT activating kinase alterations in Ph-like ALL.
Blood Adv
2017
26789921
Targeting Viral Proteostasis Limits Influenza Virus, HIV, and Dengue Virus Infection.
Immunity
2016
27935477
Regulation of B cell fate by chronic activity of the IgE B cell receptor.
Elife
2016
27821549
Mycolactone subverts immunity by selectively blocking the Sec61 translocon.
J Exp Med
2016
27768872
Chromatin Kinases Act on Transcription Factors and Histone Tails in Regulation of Inducible Transcription.
Mol Cell
2016
27863242
Decoding Mammalian Ribosome-mRNA States by Translational GTPase Complexes.
Cell
2016
27203376
Apratoxin Kills Cells by Direct Blockade of the Sec61 Protein Translocation Channel.
Cell Chem Biol
2016
27477907
Engineered Covalent Inactivation of TFIIH-Kinase Reveals an Elongation Checkpoint and Results in Widespread mRNA Stabilization.
Mol Cell
2016
27018889
Essential biphasic role for JAK3 catalytic activity in IL-2 receptor signaling.
Nat Chem Biol
2016
27056844
Phase separation of signaling molecules promotes T cell receptor signal transduction.
Science
2016
25689261
Disturbed flow-activated p90RSK kinase accelerates atherosclerosis by inhibiting SENP2 function.
J Clin Invest
2015
26485080
Corrigendum: The promise and peril of chemical probes.
Nat Chem Biol
2015
26651998
Ternatin and improved synthetic variants kill cancer cells by targeting the elongation factor-1A ternary complex.
Elife
2015
26554011
Allosteric N-WASP activation by an inter-SH3 domain linker in Nck.
Proc Natl Acad Sci U S A
2015
26006010
Prolonged and tunable residence time using reversible covalent kinase inhibitors.
Nat Chem Biol
2015
25619841
Targeting HER3 by interfering with its Sec61-mediated cotranslational insertion into the endoplasmic reticulum.
Oncogene
2015
25689339
Erratum: Covalent docking of large libraries for the discovery of chemical probes.
Nat Chem Biol
2015
24497544
An allosteric Sec61 inhibitor traps nascent transmembrane helices at the lateral gate.
Elife
2014
25344815
Covalent docking of large libraries for the discovery of chemical probes.
Nat Chem Biol
2014
25399643
Targeting protein kinases with selective and semipromiscuous covalent inhibitors.
Methods Enzymol
2014
25153195
Design of reversible, cysteine-targeted Michael acceptors guided by kinetic and computational analysis.
J Am Chem Soc
2014
23243209
A crucial role for p90RSK-mediated reduction of ERK5 transcriptional activity in endothelial dysfunction and atherosclerosis.
Circulation
2013
24085294
The prometastatic ribosomal S6 kinase 2-cAMP response element-binding protein (RSK2-CREB) signaling pathway up-regulates the actin-binding protein fascin-1 to promote tumor metastasis.
J Biol Chem
2013
1 - 50 of 102
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row(s) 1 - 30 of 30
Collaborators
Brian K Shoichet
Department of Pharmaceutical Chemistry, University of California san francisco
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Department of Pharmaceutical Chemistry, University of California san francisco
Co-authored papers
5
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University of California San Francisco
Co-authored papers
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4
Stuart L Schreiber
Broad Institute
Co-authored papers
3
Adam R Renslo
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Co-authored papers
3
Adolfo Garc??a-Sastre
Icahn School of Medicine at Mount Sinai
Co-authored papers
3
Matthew P Jacobson
Department of Pharmaceutical Chemistry, University of California san francisco
Co-authored papers
3
Phillip P Sharp
University of California san francisco
Co-authored papers
3
Wendell A Lim
University of California san francisco
Co-authored papers
2
James S Fraser
University of California san francisco
Co-authored papers
2
Jennifer L Snead
University of New Mexico Health Sciences Center
Co-authored papers
2
Philippe P Roux
IRIC - University of Montreal
Co-authored papers
2
Sagar Lonial
Co-authored papers
2
Charles S Craik
Department of Pharmaceutical Chemistry, University of California san francisco
Co-authored papers
2
Arun P Wiita
University of California San Francisco
Co-authored papers
2
Bryan L Roth
UNC Chapel Hill School of Medicine
Co-authored papers
2
Michael G Katze
University of Washington
Co-authored papers
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Nir London
The Weizmann Institute of Science
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