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Paper · 12372426

TAK1-TAB1 fusion protein: a novel constitutively active mitogen-activated protein kinase kinase kinase that stimulates AP-1 and NF-kappaB signaling pathways.

Sakurai H and 5 others. Biochem Biophys Res Commun, 2002. Cited by 74 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. TAK1-TAB1 fusion protein: a novel constitutively active mitogen-activated protein kinase kinase kinase that stimulates AP-1 and NF-kappaB signaling pathways. Papers, record 12372426. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/12372426

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Paper

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

Title
TAK1-TAB1 fusion protein: a novel constitutively active mitogen-activated protein kinase kinase kinase that stimulates AP-1 and NF-kappaB signaling pathways.
PubMed
Journal
Biochem Biophys Res Commun
PubMed
Year
2002
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
74
iCite
Relative citation ratio, by iCite
1.2
iCite
Revised in PubMed
2026-01-28
PubMed

Authors6

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

OrderAuthorForenameKindORCID iD
1Sakurai HHiroaki
2Nishi AAkito
3Sato NNaoya
4Mizukami JJunko
5Miyoshi HHidetaka
6Sugita TTakahisa

Source PubMed

Topics26

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

MeSH termMajor
Adaptor Proteins, Signal TransducingMajor topic
Carrier ProteinsMajor topic
Intracellular Signaling Peptides and ProteinsMajor topic
MAP Kinase Kinase KinasesMajor topic
NF-kappa BMajor topic
Transcription Factor AP-1Major topic
Binding Sites
Blotting, Western
DNA, Complementary
Enzyme-Linked Immunosorbent Assay
HeLa Cells
Humans
Interleukin-6
Interleukin-8
JNK Mitogen-Activated Protein Kinases
MAP Kinase Signaling System
Mitogen-Activated Protein Kinases
Models, Genetic
Mutation
Precipitin Tests
Protein Binding
Protein Structure, Tertiary
Recombinant Fusion Proteins
Transfection
p38 Mitogen-Activated Protein Kinases
MAP Kinase Kinase Kinase 7

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

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

None in this release.

Cited by35

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 74 citations.

PMIDTitleJournalYearIn PapersSource
41,581,886The stress-activated kinase p38 mediates non-canonical activation of Src and tyrosine phosphorylation of the adapter protein TAB1.J Biol Chem2026https://conductscience.org/library/papers/41581886PubMed
37,733,743Small molecule activators of TAK1 promotes its activity-dependent ubiquitination and TRAIL-mediated tumor cell death.Proc Natl Acad Sci U S A2023https://conductscience.org/library/papers/37733743PubMed
37,154,023EPRS1 Controls the TGF-β Signaling Pathway via Interaction with TβRI in Hepatic Stellate Cell.Mol Cell Biol2023https://conductscience.org/library/papers/37154023PubMed
35,459,245Supraphysiological activation of TAK1 promotes skeletal muscle growth and mitigates neurogenic atrophy.Nat Commun2022https://conductscience.org/library/papers/35459245PubMed
34,504,651Inhibition of the MAP2K7-JNK pathway with 5Z-7-oxozeaenol induces apoptosis in T-cell acute lymphoblastic leukemia.Oncotarget2021https://conductscience.org/library/papers/34504651PubMed
33,677,092mRNA-encoded, constitutively active STINGV155M is a potent genetic adjuvant of antigen-specific CD8+ T cell response.Mol Ther2021https://conductscience.org/library/papers/33677092PubMed
33,327,533TXNIP Regulates Natural Killer Cell-Mediated Innate Immunity by Inhibiting IFN-γ Production during Bacterial Infection.Int J Mol Sci2020https://conductscience.org/library/papers/33327533PubMed
32,873,150TAK1: a potent tumour necrosis factor inhibitor for the treatment of inflammatory diseases.Open Biol2020https://conductscience.org/library/papers/32873150PubMed
31,549,767A genome-wide CRISPR screen identifies FBXO42 involvement in resistance toward MEK inhibition in NRAS-mutant melanoma.Pigment Cell Melanoma Res2020https://conductscience.org/library/papers/31549767PubMed
31,214,512The MAP3K7-mTOR Axis Promotes the Proliferation and Malignancy of Hepatocellular Carcinoma Cells.Front Oncol2019https://conductscience.org/library/papers/31214512PubMed

1 to 10 of 35

See all 35 cited by

Genes6

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn GenesSource
IL63,569PubTator's text mininghttps://conductscience.org/library/genes/3569NCBI Gene
JUN3,725PubTator's text mininghttps://conductscience.org/library/genes/3725NCBI Gene
MAP3K76,885PubTator's text mininghttps://conductscience.org/library/genes/6885NCBI Gene
NFKB14,790PubTator's text mininghttps://conductscience.org/library/genes/4790NCBI Gene
TAB110,454PubTator's text mininghttps://conductscience.org/library/genes/10454NCBI Gene
WNK265,268PubTator's text mininghttps://conductscience.org/library/genes/65268NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

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

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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