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Paper216355

Reversible inhibition of skeletal muscle phosphoprotein phosphatase by ATP, phosphate and fluoride.

Khatra BS and 1 other. Biochem Biophys Res Commun, 1978. Cited by 60 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Reversible inhibition of skeletal muscle phosphoprotein phosphatase by ATP, phosphate and fluoride. Papers, record 216355. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/216355

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Reversible inhibition of skeletal muscle phosphoprotein phosphatase by ATP, phosphate and fluoride.
PubMed
Journal
Biochem Biophys Res Commun
PubMed
Year
1978
PubMed
Publication types
Journal Article, Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
60
iCite
Relative citation ratio, by iCite
1.68
iCite
Revised in PubMed
2019-06-12
PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Khatra BSB S
2Soderling TRT R

Source PubMed

Topics12

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Adenosine TriphosphateMajor topic
FluoridesMajor topic
MusclesMajor topic
PhosphatesMajor topic
Phosphoprotein PhosphatasesMajor topic
Animals
Cations, Divalent
Edetic Acid
Histones
Kinetics
Rabbits
Ribonucleotides

Source PubMed

Cited by8

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 60 citations.

PMIDTitleJournalYearIn PapersSource
36,072,300There is no F in APC: Using physiological fluoride-free solutions for high throughput automated patch clamp experiments.Front Mol Neurosci2022https://conductscience.org/library/papers/36072300PubMed
6,323,956Chromatographic characteristics and subcellular localization of synthase phosphatase, phosphorylase phosphatase and histone phosphatase in human polymorphonuclear leukocytes.Mol Cell Biochem1984https://conductscience.org/library/papers/6323956PubMed
6,278,282Inactivation and reactivation of phosphoprotein phosphatase.Mol Cell Biochem1982https://conductscience.org/library/papers/6278282PubMed
3,025,253A simple and rapid preparation of fully phosphorylated and fully dephosphorylated skeletal muscle myosin. Application to the preparation of a phosphorylated LC2-modified artificial isozyme.J Muscle Res Cell Motil1986https://conductscience.org/library/papers/3025253PubMed
2,848,509Fluorine compounds inhibit the conversion of active type-1 protein phosphatases into the ATPMg-dependent form.Biochem J1988https://conductscience.org/library/papers/2848509PubMed
2,174,099Effects of sulfhydryl agents, trifluoperazine, phosphatase inhibitors and tryptic proteolysis on calcineurin isolated from bovine cerebral cortex.Mol Cell Biochem1990https://conductscience.org/library/papers/2174099PubMed
1,903,935Characterization of Ca(2+)-dependent endogenous phosphorylation of 160,000- and 150,000-Dalton proteins of sarcoplasmic reticulum.Biochem J1991https://conductscience.org/library/papers/1903935PubMed
223,147Phosphorylation and inactivation of glycogen synthase by phosphorylase kinase.Proc Natl Acad Sci U S A1979https://conductscience.org/library/papers/223147PubMed

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

None in this release

  • Grants
  • Trials
  • Comments and corrections
  • References
  • Genes
  • Drugs
  • Data

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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