Home LiteratureArticle Details
PMID: 8622893 Published · ppublish English Journal Article

A juxtamembrane autophosphorylation site in the Eph family receptor tyrosine kinase, Sek, mediates high affinity interaction with p59fyn.

Oncogene ·Vol. 12 ·No. 8 ·1996-04-18 ·Pages 1727-36

Ellis C, Kasmi F, Ganju P, Walls E, Panayotou G, Reith AD

Abstract

The large subfamily of receptor tyrosine kinases (RTKs) for which EPH is the prototype have likely roles in intercellular communication during normal mammalian development, but the biochemical signalling pathways utilised by this family are poorly characterised. We have now identified two in vitro autophosphorylation sites within the juxtamembrane domain of the Eph family member Sek, and a candidate binding protein for the activated Sek kinase. Specific antibodies defined Sek as a 130 kDa glycoprotein with protein kinase activity expressed in keratinocytes, whilst a bacterially expressed gst-Sek kinase domain fusion protein autophosphorylated exclusively on tyrosine residues, confirming that Sek encodes an authentic protein tyrosine kinase. Two dimensional phosphopeptide mapping and site-directed mutagenesis defined juxtamembrane residue Y602 as a major site of in vitro autophosphorylation in Sek, whilst Y596 was phosphorylated to a lower stoichiometry. Complimentary approaches of in vitro binding assays and BIAcore analysis revealed a high affinity association between the Y602 Sek autophosphorylation site and the cytoplasmic tyrosine kinase p59fyn, an interaction mediated through the SH2 domain of this intracellular signalling molecule. Moreover, these data identify the novel phosphotyrosyl motif pYEDP as mediating high affinity association with fyn-SH2, extending the previously defined consensus motif for this interaction. The extensive conservation of this fyn-binding motif within the juxtamembrane domain of Eph family RTKs suggests that signalling through fyn, or fyn-related, tyrosine kinases may be utilised by many members of this large subclass of transmembrane receptors.

MeSH Terms
Amino Acid Sequence Amino Acids/analysis Animals Bacterial Proteins/genetics,metabolism Binding Sites Cells, Cultured Conserved Sequence Fetal Proteins/chemistry,genetics,metabolism Glutathione Transferase/genetics,metabolism Glycoproteins/chemistry,metabolism Keratinocytes/cytology Molecular Sequence Data Peptide Fragments/chemistry,genetics,metabolism Phosphorylation Proto-Oncogene Proteins/chemistry,metabolism Proto-Oncogene Proteins c-fyn Receptor Protein-Tyrosine Kinases/chemistry,genetics,metabolism Receptor, EphA4 Recombinant Fusion Proteins/genetics,metabolism Sequence Homology, Amino Acid Signal Transduction Time Factors src Homology Domains
Chemicals
Amino Acids Bacterial Proteins Fetal Proteins Glycoproteins Peptide Fragments Proto-Oncogene Proteins Recombinant Fusion Proteins Glutathione Transferase Receptor Protein-Tyrosine Kinases Receptor, EphA4 Proto-Oncogene Proteins c-fyn
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Ellis C
Institute of Cancer Research, Chester Beatty Laboratories, London, UK.
Kasmi F
Ganju P
Walls E
Panayotou G
Reith A D
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1996-04-18
Pages
1727-36
Language
English
Region
England
NLM ID
8711562
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com