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Article

The multisubstrate docking site of the MET receptor is dispensable for MET-mediated RAS signaling and cell scattering.

Molecular biology of the cell - 1 Mar 1999

Tulasne D, Paumelle R, Weidner K M, Vandenbunder B, Fafeur V

Abstract excerpt

The scatter factor/hepatocyte growth factor regulates scattering and morphogenesis of epithelial cells through activation of the MET tyrosine kinase receptor. In particular, the noncatalytic C-terminal tail of MET contains two autophosphorylation tyrosine residues, which form a multisubstrate-bin...

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Topics

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Share to Adaptor Proteins, Vesicular Transport
Share to Hepatocyte Growth Factor
Share to Phosphatidylinositol 3-Kinases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Proto-Oncogene Proteins c-ets

Share to Proto-Oncogene Proteins c-met

Share to Shc Signaling Adaptor Proteins

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Source

Open in PubMed Open full text

Identifiers

PMID: 10069803
DOI: 10.1091/mbc.10.3.551
PMCID: PMC25187

Genes

MET
GAB1
GRB2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10069803-2026-09-02.1. Manifest publication-graph-cohort-2026-09-02.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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The multisubstrate docking site of the MET receptor is dispensable for MET-mediated RAS signaling and cell scattering.PMID 10069803Read ↗

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