Evidence map›Paper›PMID 20093729›Full record

ArticleGeneral physiology and biophysics2009

Novel protein ligands of the annexin A7 N-terminal region suggest pro-beta helices engage one another with high specificity.

Carl E Creutz

Abstract read
In one paragraph

Article in General physiology and biophysics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 84% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

1 author at 1 institution in 1 country.

Carl E CreutzDepartment of Pharmacology, University of Virginia, Charlottesville, VA 22908, USA. Creutz@virginia.edu
University of Virginia · US

Funding

ANNEXIN PHOSPHORYLATION: CAUSES AND CONSEQUENCESR01GM059891 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI CREUTZ, CARL E · 2001 to 2004
$884k
NIGMS NIH HHS R01 GM059891NIGMS NIH HHS R01GM59891
6 · The paper itself

Abstract

The N-terminal regions of annexins A7 (synexin) and A11 consist of an extended series of short sequence repeats rich in tyrosine, proline, and glycine that provide binding sites for other proteins that may be recruited to membranes by the annexins and that may modulate the calcium and membrane binding activities of the annexin core domains. In this study two new ligands for the annexin A7 N terminal region were identified by yeast two hybrid screening: the TNFalpha receptor regulatory protein SODD (Suppressor Of Death Domains) and KIAA0280, a protein of unknown function. Strikingly, the sites of interaction of these proteins with the annexin also contain sequence repeats similar to those present in the N-termini of annexins A7 and A11. It was also found that the annexin A7 N-terminal region interacts with itself in the two hybrid assay. These results suggest that sequence repeats of this nature form novel structures, called YP pro-beta helices, that are characterized by an ability to interact with one another. Specificity of interactions between the pro-beta helices in different proteins may be encoded by the variations of residues and lengths of the sequence repeats.

Indexed as

Amino Acid MotifsAmino Acid SequenceAnimalsAnnexin A7AnnexinsBinding SitesGene LibraryHumansLigandsMiceMolecular Sequence DataProtein BindingProtein Structure, SecondaryProtein Structure, TertiaryTwo-Hybrid System TechniquesAnnexin A7AnnexinsLigands

Identifiers

PMID20093729
PMCPMC2931597
OpenAlexW2133102895

What OpenQuestion holds

Textmetadata
LicenceTDM
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.