Evidence map›Paper›PMID 9730898›Full record

ArticleThe Journal of experimental medicine1998

Qa-1b binds conserved class I leader peptides derived from several mammalian species.

Z Kurepa, C A Hasemann, J Forman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 84 citations in OpenAlex.

  1. The murine MHC-E molecule Qa-1Frontiers in immunology · 2026
    Article
  2. Article
  3. Qa-1Molecular cancer research : MCR · 2021
    Article
  4. Article
  5. Targeting Innate-Like T Cells in Tuberculosis.Frontiers in immunology · 2016
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. MR1 antigen presentation to mucosal-associated invariant T cells was highly conserved in evolution.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  11. Article
  12. Perceiving the avidity of T cell activation can be translated into peripheral T cell regulation.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Article
  13. Review
  14. An affinity/avidity model of peripheral T cell regulation.The Journal of clinical investigation · 2005
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. CD8+ T cells control the TH phenotype of MBP-reactive CD4+ T cells in EAE mice.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Z KurepaImmunology Graduate Program, University of Texas Southwestern Medical Center at Dallas 75235, USA.
C A Hasemann
J Forman
The University of Texas Southwestern Medical Center · US

Funding

STRUCTURE AND FUNCTION OF MHC CLASS IB HAPLOTYPESP01AI037818 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI FORMAN, JAMES M · 1995 to 2002
$1.9M
ANTIGEN PRESENTATION BY CLASS IB MOLECULE, QA-1R01AI034930 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI FORMAN, JAMES M · 1995 to 2004
$1.3M
ROLE OF CLASS IB ANTIGENS AND OPPORTUNISTIC INFECTIONSR01AI037942 · NIAID · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI FORMAN, JAMES M · 1995 to 1999
–
NIAID NIH HHS 5-RO1-AI-37942NIAID NIH HHS P01-AI-37818NIAID NIH HHS R01 AI034930NIAID NIH HHS R01-AI-34930
6 · The paper itself

Abstract

Qa-1b binds a peptide (AMAPRTLLL), referred to as Qdm (for Qa-1 determinant modifier), derived from the signal sequence of murine class Ia molecules. This peptide binds with high affinity and accounts for almost all of the peptides associated with this molecule. Human histocompatibility leukocyte antigen (HLA)-E, a homologue of Qa-1b, binds similar peptides derived from human class Ia molecules and interacts with CD94/NKG2 receptors on natural killer cells. We used surface plasmon resonance to determine the ability of Qa-1b to bind related ligands representing peptides derived from the leaders of class I molecules from several mammalian species. All of the peptides reported to bind HLA-E bound readily to Qa-1b. In addition, peptides derived from leader segments of different mammals also bound to Qa-1b, indicating a conservation of this "Qdm-like" epitope throughout mammalian evolution. We have attempted to define a minimal peptide on a polyglycine backbone that binds Qa-1b. Our previous findings showed that P2 and P9 are important but not sufficient for binding to Qa-1b. Although a minimum peptide (GMGGGGLLL) bound Qa-1(b), its interaction was relatively weak, as were peptides sharing five or six residues with Qdm, indicating that multiple native residues are required for a strong interaction. This finding is consistent with the observation that this molecule preferentially binds this single ligand.

Indexed as

Amino Acid SequenceAnimalsCatsCattleCell LineConserved SequenceDogsDose-Response Relationship, ImmunologicDrosophila melanogasterGorilla gorillaHistocompatibility Antigens Class IHLA AntigensHLA-E AntigensHumansMiceMice, Inbred C57BLHistocompatibility Antigens Class IHLA AntigensHLA-E AntigensPeptide FragmentsPeptidesProtein Sorting SignalsQdm protein, mouseQ surface antigens

Identifiers

PMID9730898
PMCPMC2213384
OpenAlexW1993295071

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.