Recognition of multiple substrate motifs by the c-ABL protein tyrosine kinase

被引:22
作者
Wu, JJ
Afar, DEH
Phan, H
Witte, ON
Lam, KS
机构
[1] Univ Calif Davis, US Davis Danc Ctr, Dept Internal Med, Div Hematol Oncol, Sacramento, CA 95817 USA
[2] Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Howard Hughes Med Inst, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90095 USA
关键词
D O I
10.2174/1386207023330516
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Using a combinatorial peptide library that is based on the one-bead one-peptide approach we identified 14 peptide substrates for the c-ABL protein tyrosine kinase, which define three distinct consensus sequence groups. This is distinct from many serine/threonine kinases, which often phosphorylate only one major consensus sequence. The three consensus sequences accurately predict phosphorylation sites in cellular ABL substrates proven to play a role in cell signaling. Our data suggest that protein tyrosine kinases have evolved to recognize multiple substrate motifs.
引用
收藏
页码:83 / 91
页数:9
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共 76 条
[11]   C-Abl-induced apoptosis, but not cell cycle arrest, requires mitogen-activated protein kinase kinase 6 activation [J].
Cong, F ;
Goff, SP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :13819-13824
[12]   ABI-2, A NOVEL SH3-CONTAINING PROTEIN INTERACTS WITH THE C-ABL TYROSINE KINASE AND MODULATES C-ABL TRANSFORMING ACTIVITY [J].
DAI, ZH ;
PENDERGAST, AM .
GENES & DEVELOPMENT, 1995, 9 (21) :2569-2582
[13]   INDUCTION OF CHRONIC MYELOGENOUS LEUKEMIA IN MICE BY THE P210BCR/ABL GENE OF THE PHILADELPHIA-CHROMOSOME [J].
DALEY, GQ ;
VANETTEN, RA ;
BALTIMORE, D .
SCIENCE, 1990, 247 (4944) :824-830
[14]   PHOSPHORYLATION OF GAP AND GAP-ASSOCIATED PROTEINS BY TRANSFORMING AND MITOGENIC TYROSINE KINASES [J].
ELLIS, C ;
MORAN, M ;
MCCORMICK, F ;
PAWSON, T .
NATURE, 1990, 343 (6256) :377-381
[15]   DELETION OF AN N-TERMINAL REGULATORY DOMAIN OF THE C-ABL TYROSINE KINASE ACTIVATES ITS ONCOGENIC POTENTIAL [J].
FRANZ, WM ;
BERGER, P ;
WANG, JYJ .
EMBO JOURNAL, 1989, 8 (01) :137-147
[16]   GENERAL-METHOD FOR RAPID SYNTHESIS OF MULTICOMPONENT PEPTIDE MIXTURES [J].
FURKA, A ;
SEBESTYEN, F ;
ASGEDOM, M ;
DIBO, G .
INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH, 1991, 37 (06) :487-493
[17]   TYROSINE-PHOSPHORYLATED PROTEINS - MEDIATORS OF SIGNAL TRANSDUCTION FROM THE TYROSINE KINASES [J].
GLENNEY, JR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1134 (02) :113-127
[18]   STRUCTURE OF THE ABELSON MURINE LEUKEMIA-VIRUS GENOME AND THE HOMOLOGOUS CELLULAR GENE - STUDIES WITH CLONED VIRAL-DNA [J].
GOFF, SP ;
GILBOA, E ;
WITTE, ON ;
BALTIMORE, D .
CELL, 1980, 22 (03) :777-785
[19]   ALTERNATIVE SIGNALS TO RAS FOR HEMATOPOIETIC TRANSFORMATION BY THE BCR-ABL ONCOGENE [J].
GOGA, A ;
MCLAUGHLIN, J ;
AFAR, DEH ;
SAFFRAN, DC ;
WITTE, ON .
CELL, 1995, 82 (06) :981-988
[20]   ONCOGENIC ACTIVATION OF C-ABL BY MUTATION WITHIN ITS LAST EXON [J].
GOGA, A ;
MCLAUGHLIN, J ;
PENDERGAST, AM ;
PARMAR, K ;
MULLER, A ;
ROSENBERG, N ;
WITTE, ON .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :4967-4975