Evidence map›Paper›PMID 10498863›Full record

ArticleOncogene1999

Drosophila abelson interacting protein (dAbi) is a positive regulator of abelson tyrosine kinase activity.

J L Juang, F M Hoffmann

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Oncogene, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Adaptor protein Abelson interactor 1 in homeostasis and disease.Cell communication and signaling : CCS · 2024
    Review
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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

2 authors at 2 institutions in 2 countries.

J L JuangNational Health Research Institute, 128 Yen-Chiu-Yuan Road, Sec. 2, Taipei, Taiwan.
F M Hoffmann
National Health Research Institutes · TWUniversity of Wisconsin–Madison · US

Funding

GENETIC ANALYSIS OF DROSOPHILA ABELSON TYROSINE KINASER01CA049582 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI HOFFMANN, F. MICHAEL · 1989 to 1998
–
NCI NIH HHS CA49582
6 · The paper itself

Abstract

Human and mouse Abelson interacting proteins (Abi) are SH3-domain containing proteins that bind to the proline-rich motifs of the Abelson protein tyrosine kinase. We report a new member of this gene family, a Drosophila Abi (dAbi) that is a substrate for Abl kinase and that co-immunoprecipitates with Abl if the Abi SH3 domain is intact. We have identified a new function for both dAbi and human Abi-2 (hAbi-2). Both proteins activate the kinase activity of Abl as assayed by phosphorylation of the Drosophila Enabled (Ena) protein. Removal of the dAbi SH3 domain eliminates dAbi's activation of Abl kinase activity. dAbi is an unstable protein in cells and is present at low steady state levels but its protein level is increased coincident with phosphorylation by Abl kinase. Expression of the antisense strand of dAbi reduces dAbi protein levels and abolishes activation of Abl kinase activity. Modulation of Abi protein levels may be an important mechanism for regulating the level of Abl kinase activity in the cell.

Indexed as

Adaptor Proteins, Signal TransducingCytoskeletal ProteinsDrosophila ProteinsAbelson murine leukemia virusAmino Acid SequenceAnimalsCarrier ProteinsCloning, MolecularConsensus SequenceDrosophila melanogasterEnzyme ActivationEvolution, MolecularHomeodomain ProteinsHumansInsect ProteinsMiceABI1 protein, humanAbi1 protein, mouseABI2 protein, humanAbi protein, DrosophilaAdaptor Proteins, Signal TransducingCarrier ProteinsCytoskeletal ProteinsDrosophila ProteinsHomeodomain ProteinsInsect ProteinsOncogene Proteins v-ablProtein-Tyrosine KinasesProto-Oncogene Proteins c-abl

Identifiers

PMID10498863
OpenAlexW2030112336

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.