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
相关论文
共 76 条
[21]   Protein binding and signaling properties of RIN1 suggest a unique effector function [J].
Han, LM ;
Wong, D ;
Dhaka, A ;
Afar, D ;
White, M ;
Xie, WL ;
Herschman, H ;
Witte, O ;
Colicelli, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :4954-4959
[22]   GENERATION AND USE OF SYNTHETIC PEPTIDE COMBINATORIAL LIBRARIES FOR BASIC RESEARCH AND DRUG DISCOVERY [J].
HOUGHTEN, RA ;
PINILLA, C ;
BLONDELLE, SE ;
APPEL, JR ;
DOOLEY, CT ;
CUERVO, JH .
NATURE, 1991, 354 (6348) :84-86
[23]   STY, A TYROSINE-PHOSPHORYLATING ENZYME WITH SEQUENCE HOMOLOGY TO SERINE THREONINE KINASES [J].
HOWELL, BW ;
AFAR, DEH ;
LEW, J ;
DOUVILLE, EMJ ;
ICELY, PLE ;
GRAY, DA ;
BELL, JC .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (01) :568-572
[24]  
HOWELL BW, 1991, SEMINARS DEV BIOL, V2, P345
[25]   CRYSTAL-STRUCTURE OF THE TYROSINE KINASE DOMAIN OF THE HUMAN INSULIN-RECEPTOR [J].
HUBBARD, SR ;
WEI, L ;
ELIS, L ;
HENDRICKSON, WA .
NATURE, 1994, 372 (6508) :746-754
[26]   N-TERMINAL MUTATIONS ACTIVATE THE LEUKEMOGENIC POTENTIAL OF THE MYRISTOYLATED FORM OF C-ABL [J].
JACKSON, P ;
BALTIMORE, D .
EMBO JOURNAL, 1989, 8 (02) :449-456
[27]   PROTEIN-KINASE RECOGNITION SEQUENCE MOTIFS [J].
KEMP, BE ;
PEARSON, RB .
TRENDS IN BIOCHEMICAL SCIENCES, 1990, 15 (09) :342-346
[28]  
KEMP BE, 1977, J BIOL CHEM, V252, P4888
[29]   STRUCTURE OF A PEPTIDE INHIBITOR BOUND TO THE CATALYTIC SUBUNIT OF CYCLIC ADENOSINE-MONOPHOSPHATE DEPENDENT PROTEIN-KINASE [J].
KNIGHTON, DR ;
ZHENG, JH ;
TENEYCK, LF ;
XUONG, NH ;
TAYLOR, SS ;
SOWADSKI, JM .
SCIENCE, 1991, 253 (5018) :414-420
[30]   AN ALTERATION OF THE HUMAN C-ABL PROTEIN IN K562 LEUKEMIA-CELLS UNMASKS ASSOCIATED TYROSINE KINASE-ACTIVITY [J].
KONOPKA, JB ;
WATANABE, SM ;
WITTE, ON .
CELL, 1984, 37 (03) :1035-1042