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PMID: 9008161 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Identification of the Abl- and rasGAP-associated 62 kDa protein as a docking protein, Dok.

Cell ·Vol. 88 ·No. 2 ·1997-01-24 ·Pages 205-11

Yamanashi Y, Baltimore D

Abstract

A 62 kDa protein is highly phosphorylated in many cells containing activated tyrosine kinases. This protein, characterized mainly by its avid association with rasGAP, has proved elusive. Anti-phosphotyrosine antibody was used to purify p62. From peptide sequence, molecular cloning revealed a cDNA encoding a novel protein, p62dok, with little homology to others but with a prominent set of tyrosines and nearby sequences suggestive of SH2 binding sites. In cells, v-Abl tyrosine kinase binds and strongly phosphorylates p62dok, which then binds rasGAP. A monoclonal antibody, 2C4, to the rasGAP-associated p62 reacts with p62dok. Thus, p62dok appears to be the long-sought major substrate of many tyrosine kinases.

MeSH Terms
Amino Acid Sequence Animals Antibodies, Monoclonal/immunology Binding Sites Blotting, Northern Cell Line Cell Line, Transformed Cloning, Molecular DNA, Complementary/genetics DNA-Binding Proteins/immunology GTPase-Activating Proteins Mice Molecular Sequence Data Oncogene Proteins v-abl/metabolism Phosphoproteins/chemistry,genetics,immunology,isolation & purification,metabolism Phosphorylation Phosphotyrosine/metabolism Protein-Tyrosine Kinases/metabolism Proteins/metabolism RNA-Binding Proteins/immunology Sequence Homology, Amino Acid Transfection src Homology Domains
Chemicals
Antibodies, Monoclonal DNA, Complementary DNA-Binding Proteins Dok1 protein, mouse GAP-associated protein p62 GTPase-Activating Proteins Oncogene Proteins v-abl Phosphoproteins Proteins RNA-Binding Proteins Phosphotyrosine Protein-Tyrosine Kinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Yamanashi Y
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139, USA.
Baltimore D
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1997-01-24
Pages
205-11
Language
English
Region
United States
NLM ID
0413066
Subset
IM
Grants
NCI NIH HHS · CA-51462 · United States
Databases
GENBANK
U78818
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