Evidence map›Paper›PMID 1731338›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1992

Amino acid sequence of human plasma galactoglycoprotein: identity with the extracellular region of CD43 (sialophorin).

K Schmid, M A Hediger, R Brossmer, J H Collins, H Haupt, T Marti, G D Offner, J Schaller, K Takagaki, M T Walsh

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1992. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. CD43, a molecule with multiple functions.Immunologic research · 1999
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

10 authors at 1 institution in 1 country.

K SchmidDepartment of Biochemistry, Boston University School of Medicine, MA 02118.
M A Hediger
R Brossmer
J H Collins
H Haupt
T Marti
G D Offner
J Schaller
K Takagaki
M T Walsh
Boston University · US

Funding

ROLE OF MACROPHAGE SIALOPHORIN (CD43) IN HIV DEFENSER01AI029880 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI REMOLD-O'DONNELL, EILEEN · 1990 to 1992
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MOLECULAR BIOLOGY OF BRUSH BORDER TRANSPORT PROTEINSR01DK043171 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI HEDIGER, MATTHIAS A · 1990 to 1999
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CHEMISTRY OF HUMAN PROTEINS AND GLYCOPROTEINSR01GM010374 · NIGMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SCHMID, KARL · 1985 to 1987
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NIAID NIH HHS AI29880NIDDK NIH HHS DK-43171NIGMS NIH HHS GM-10374
6 · The paper itself

Abstract

The amino acid sequence of galactoglycoprotein purified from human plasma was elucidated to 75% completeness by using chemical degradation of peptides and glycopeptides derived from digests of the protein with seven specific proteases. This sequence represents a polypeptide chain of approximately 220 amino acid residues including a high content of serine, threonine, alanine, and proline with one N-linked and multiple O-linked glycans. Comparison of peptide sequences from the native galactoglycoprotein and the deglycosylated derivative demonstrated the locations of 25 sites of O-glycosylation and three serine sites that are not glycosylated. The homogeneous N terminus was established as serine. C-terminal analysis revealed multiple C-terminal residues, suggesting that galactoglycoprotein molecules are of varying lengths. A search of a protein data base revealed that the galactoglycoprotein polypeptide is identical to the N-terminal (extracellular) polypeptide region of the blood-cell surface molecule CD43 (sialophorin, leukosialin). Further support of the relatedness of these molecules was obtained by immunoprecipitation of 125I-labeled galactoglycoprotein by monoclonal anti-CD43 antibodies. The composition and properties of the molecules together with the known structure of the gene encoding CD43 suggest that galactoprotein is derived by proteolytic cleavage from transmembrane "hexasaccharide CD43," known to be expressed on neutrophils, activated T lymphocytes, and platelets.

Indexed as

Amino Acid SequenceAntigens, CDBlood ProteinsCarbohydrate SequenceGlycopeptidesGlycoproteinsHumansLeukosialinMolecular Sequence DataMolecular WeightPeptide FragmentsProtein ConformationSialoglycoproteinsAntigens, CDBlood ProteinsGlycopeptidesGlycoproteinsLeukosialinPeptide FragmentsSialoglycoproteinsSPN protein, human

Identifiers

PMID1731338
PMCPMC48299
OpenAlexW2020139747

What OpenQuestion holds

Textmetadata
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.