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Paper162829

Rabbit skeletal muscle protein kinase. Conversion from cAMP dependent to independent form by chemical perturbations.

Huang LC and 1 other. Biochemistry, 1975. Cited by 44 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Rabbit skeletal muscle protein kinase. Conversion from cAMP dependent to independent form by chemical perturbations. Papers, record 162829. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/162829

Paper

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

Title
Rabbit skeletal muscle protein kinase. Conversion from cAMP dependent to independent form by chemical perturbations.
PubMed
Journal
Biochemistry
PubMed
Year
1975
PubMed
Publication types
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
44
iCite
Relative citation ratio, by iCite
1.32
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
1Huang LCL C
2Huang CC

Source PubMed

Topics11

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

MeSH termMajor
Cyclic AMPMajor topic
MusclesMajor topic
Protein KinasesMajor topic
Animals
Enzyme Activation
Macromolecular Substances
Molecular Weight
Rabbits
Thiocyanates
Trypsin
Urea

Source PubMed

Cited by9

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 44 citations.

PMIDTitleJournalYearIn PapersSource
7,458,911Isolation and some properties of troponin T kinase from rabbit skeletal muscle.Biochem J1980https://conductscience.org/library/papers/7458911PubMed
6,307,258Chemical cross-linking of cyclic AMP-dependent protein kinase and its dissimilar subunits.Biochem J1983https://conductscience.org/library/papers/6307258PubMed
6,302,672cAMP-dependent protein kinase phosphorylates the nicotinic acetylcholine receptor.Proc Natl Acad Sci U S A1983https://conductscience.org/library/papers/6302672PubMed
6,249,267
Modification and identification of glutamate residues at the arginine-recognition site in the catalytic subunit of adenosine 3' :5'-cyclic monophosphate-dependent protein kinase of rabbit skeletal muscle.
Biochem J1980https://conductscience.org/library/papers/6249267PubMed
225,657Regulatory and functional compartment of three multifunctional protein kinase systems.Mol Cell Biochem1979https://conductscience.org/library/papers/225657PubMed
212,013Evidence for an essential arginine recognition site on adenosine 3':5'-cyclic monophosphate-dependent protein kinase of rabbit skeletal muscle.Biochem J1978https://conductscience.org/library/papers/212013PubMed
200,226Binding proteins for adenosine 3':5'-cyclic monophosphate in bovine adrenal cortex.Biochem J1977https://conductscience.org/library/papers/200226PubMed
192,203Factors affecting the binding of [3H]adenosine 3':5'-cyclic monophosphate to protein kinase from bovine adrenal cortex.Biochem J1977https://conductscience.org/library/papers/192203PubMed
191,831Subunit interaction in cyclic AMP-dependent protein kinase of mutant lymphoma cells.Proc Natl Acad Sci U S A1977https://conductscience.org/library/papers/191831PubMed

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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