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Paper6089752

The allosteric properties of rat liver fructose-1,6-bisphosphatase.

Meek DW and 1 other. Biochem J, 1984. Cited by 20 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. The allosteric properties of rat liver fructose-1,6-bisphosphatase. Papers, record 6089752. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/6089752

Paper

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

Title
The allosteric properties of rat liver fructose-1,6-bisphosphatase.
PubMed
Journal
Biochem J
PubMed
Year
1984
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
20
iCite
Relative citation ratio, by iCite
0.72
iCite
Revised in PubMed
2019-05-01
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Meek DWD W
2Nimmo HGH G

Source PubMed

Topics13

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

MeSH termMajor
Fructose-BisphosphataseMajor topic
LiverMajor topic
Adenosine Monophosphate
Allosteric Regulation
Animals
Enzyme Activation
Fructosediphosphates
Kinetics
Magnesium
Models, Biological
Phosphorylation
Rats
Rats, Inbred Strains

Source PubMed

References19

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
114,343,300ON THE NATURE OF ALLOSTERIC TRANSITIONS: A PLAUSIBLE MODEL.J Mol Biol1965https://conductscience.org/library/papers/14343300PubMed
214,275,118ALLOSTERIC INHIBITION OF RAT LIVER FRUCTOSE 1,6-DIPHOSPHATASE BY ADENOSINE 5'-MONOPHOSPHATE.J Biol Chem1965https://conductscience.org/library/papers/14275118PubMed
35,036,459A multichamber equilibrium dialysis apparatus.Anal Biochem1972https://conductscience.org/library/papers/5036459PubMed
4241,647The effect of pH on the kinetics of beef-liver fructose bisphosphatase.Eur J Biochem1975https://conductscience.org/library/papers/241647PubMed
5171,160The allosteric properties of beef-liver fructose bisphosphatase.Eur J Biochem1975https://conductscience.org/library/papers/171160PubMed
611,750The purification of properties of rat liver fructose 1,6-bisphosphatase.Arch Biochem Biophys1976https://conductscience.org/library/papers/11750PubMed
76,260,770Inhibition of fructose-1,6-bisphosphatase by fructose 2,6-bisphosphate.J Biol Chem1981https://conductscience.org/library/papers/6260770PubMed
86,265,919Inhibition of fructose-1,6-bisphosphatase by fructose 2,6-biphosphate.Proc Natl Acad Sci U S A1981https://conductscience.org/library/papers/6265919PubMed
96,271,753The role of fructose 2,6-bisphosphate in regulation of fructose-1,6-bisphosphatase.J Biol Chem1981https://conductscience.org/library/papers/6271753PubMed
106,282,868Studies on the mechanism of interaction of fructose 2,6-bisphosphate with fructose-1,6-bisphosphatase.J Biol Chem1982https://conductscience.org/library/papers/6282868PubMed
116,297,401On the mechanism of inhibition of fructose 1,6-bisphosphatase by fructose 2,6-bisphosphate.Arch Biochem Biophys1982https://conductscience.org/library/papers/6297401PubMed
126,307,691On the mechanism of inhibition of neutral liver fructose 1,6-bisphosphatase by fructose 2,6-bisphosphate.Eur J Biochem1983https://conductscience.org/library/papers/6307691PubMed
136,309,560The interaction of fructose 2,6-bisphosphate with an allosteric site of rat liver fructose 1,6-bisphosphatase.FEBS Lett1983https://conductscience.org/library/papers/6309560PubMed
146,688,419The interaction of fructose 2,6-bisphosphate and AMP with rat hepatic fructose 1,6-bisphosphatase.J Biol Chem1983https://conductscience.org/library/papers/6688419PubMed
156,577,418Allosteric cofactor-mediated enzyme cooperativity: a theoretical treatment.Proc Natl Acad Sci U S A1983https://conductscience.org/library/papers/6577418PubMed
166,311,081Gluconeogenesis and related aspects of glycolysis.Annu Rev Biochem1983https://conductscience.org/library/papers/6311081PubMed
176,321,240Biphasic effect of fructose 2,6-bisphosphate on the liver fructose-1,6-bisphosphatase: mechanistic and physiological implications.FEBS Lett1984https://conductscience.org/library/papers/6321240PubMed
186,089,751Effects of phosphorylation on the kinetic properties of rat liver fructose-1,6-bisphosphatase.Biochem J1984https://conductscience.org/library/papers/6089751PubMed
195,972,463On the nature of allosteric transitions: implications of non-exclusive ligand binding.J Mol Biol1966https://conductscience.org/library/papers/5972463PubMed

Cited by3

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 20 citations.

PMIDTitleJournalYearIn PapersSource
19,587,243Fasting hyperglycemia is not associated with increased expression of PEPCK or G6Pc in patients with Type 2 Diabetes.Proc Natl Acad Sci U S A2009https://conductscience.org/library/papers/19587243PubMed
7,575,399Kinetic properties of D-fructose-1,6-bisphosphate 1-phosphohydrolase isolated from human muscle.Biochem J1995https://conductscience.org/library/papers/7575399PubMed
6,089,751Effects of phosphorylation on the kinetic properties of rat liver fructose-1,6-bisphosphatase.Biochem J1984https://conductscience.org/library/papers/6089751PubMed

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
  • 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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