Cited by 50Protein Tyrosine PhosphatasesRedox biology and oxidative stressProtein Kinase Regulation and GTPase Signaling

[29] Redox regulation of protein tyrosine phosphatases by hydrogen peroxide: Detecting sulfenic acid intermediates and examining reversible inactivation

Denu, John M., Tanner, Kirk G.·2002·Methods in Enzymology

Integrity signals

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Crossref · 10.1016/s0076-6879(02)48648-x

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14 of 14 references verified0 citation errors · 0 not checkable

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  • The phosphatases that negatively modulate the insulin pathway are the main targets for oxidative inhibition by ROS.

    “In particular, the phosphatases that negatively modulate the insulin pathway are the main targets for oxidative inhibition by ROS ([35](#B35)).”

    From Mitochondrial fatty acid oxidation in obesity (2013) · cites this paper as [35]

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Authors
Denu, J. M., & Tanner, K. G.
Affiliations
Oregon Health & Science University (US)
Venue
Methods in Enzymology
Publisher
Elsevier
Published
2002
Volume
348
Pages
297-305
ISSN
0076-6879 (ISSN-L)
OpenAlex
W1668328580
Cited by
50
References
14
Citations by year
2022: 1 · 2021: 2 · 2019: 1 · 2018: 2 · 2017: 2 · 2015: 2 · 2014: 2 · 2013: 3 · 2012: 2
FWCI
5.32
Type
book chapter
Language
en
Open access
closed
Locations
  • Methods in enzymology on CD-ROM/Methods in enzymology (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of General Medical Sciences (GM59785-01)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords
protein tyrosine phosphatase, hydrogen peroxide, sulfenic acid, redox regulation, reversible inactivation, growth factor signaling, cell surface receptors
MeSH terms
Cell Line, Cysteine, Enzyme Inhibitors, Epidermal Growth Factor, Glutathione, Humans, Hydrogen Peroxide, Hydrogen-Ion Concentration, Kinetics, Models, Biological, 4-Chloro-7-nitrobenzofurazan, Oxidation-Reduction, Sulfenic Acids, Signal Transduction, Protein Tyrosine Phosphatases, Catalytic Domain

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