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Paper · 2137462

Lysine 271 in the transmembrane domain of the T-cell antigen receptor beta chain is necessary for its assembly with the CD3 complex but not for alpha/beta dimerization.

Alcover A and 3 others. J Biol Chem, 1990. Cited by 85 papers, by iCite.

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ConductScience Library. Lysine 271 in the transmembrane domain of the T-cell antigen receptor beta chain is necessary for its assembly with the CD3 complex but not for alpha/beta dimerization. Papers, record 2137462. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/2137462

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Paper

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

Title
Lysine 271 in the transmembrane domain of the T-cell antigen receptor beta chain is necessary for its assembly with the CD3 complex but not for alpha/beta dimerization.
PubMed
Journal
J Biol Chem
PubMed
Year
1990
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
85
iCite
Relative citation ratio, by iCite
1.25
iCite
Revised in PubMed
2021-02-10
PubMed

Authors4

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

OrderAuthorForenameKindORCID iD
1Alcover AA
2Mariuzza RAR A
3Ermonval MM
4Acuto OO

Source PubMed

Topics18

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

MeSH termMajor
Antigens, CDMajor topic
Antigens, Differentiation, T-LymphocyteMajor topic
LysineMajor topic
Receptors, Antigen, T-CellMajor topic
Base Sequence
CD3 Complex
Cell Membrane
Cloning, Molecular
Genes
Humans
Macromolecular Substances
Membrane Glycoproteins
Molecular Sequence Data
Mutation
Oligonucleotide Probes
Restriction Mapping
T-Lymphocytes
Transfection

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 by34

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 85 citations.

PMIDTitleJournalYearIn PapersSource
41,865,294Membrane-Based Assembly and Interactions in Immune Receptors.Chem Rev2026https://conductscience.org/library/papers/41865294PubMed
39,745,432Biophysical and Structural Features of αβT-Cell Receptor Mechanosensing: A Paradigmatic Shift in Understanding T-Cell Activation.Immunol Rev2025https://conductscience.org/library/papers/39745432PubMed
34,260,912Allosteric activation of T cell antigen receptor signaling by quaternary structure relaxation.Cell Rep2021https://conductscience.org/library/papers/34260912PubMed
30,877,195Lysosomal targeting of the ABC transporter TAPL is determined by membrane-localized charged residues.J Biol Chem2019https://conductscience.org/library/papers/30877195PubMed
30,815,789NMR: an essential structural tool for integrative studies of T cell development, pMHC ligand recognition and TCR mechanobiology.J Biomol NMR2019https://conductscience.org/library/papers/30815789PubMed
30,389,415The T Cell Antigen Receptor α Transmembrane Domain Coordinates Triggering through Regulation of Bilayer Immersion and CD3 Subunit Associations.Immunity2018https://conductscience.org/library/papers/30389415PubMed
25,947,381Impact of Exogenous Galectin-9 on Human T Cells: CONTRIBUTION OF THE T CELL RECEPTOR COMPLEX TO ANTIGEN-INDEPENDENT ACTIVATION BUT NOT TO APOPTOSIS INDUCTION.J Biol Chem2015https://conductscience.org/library/papers/25947381PubMed
24,488,493Structure of the chicken CD3εδ/γ heterodimer and its assembly with the αβT cell receptor.J Biol Chem2014https://conductscience.org/library/papers/24488493PubMed
24,454,946Lck mediates signal transmission from CD59 to the TCR/CD3 pathway in Jurkat T cells.PLoS One2014https://conductscience.org/library/papers/24454946PubMed
23,133,531Diversity, molecular characterization and expression of T cell receptor γ in a teleost fish, the sea bass (Dicentrarchus labrax, L).PLoS One2012https://conductscience.org/library/papers/23133531PubMed

1 to 10 of 34

See all 34 cited by

Genes3

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
APP351PubTator's text mininghttps://conductscience.org/library/genes/351NCBI Gene
EDNRA1,909PubTator's text mininghttps://conductscience.org/library/genes/1909NCBI Gene
TRB6,957PubTator's text mininghttps://conductscience.org/library/genes/6957NCBI 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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