Crk and CrkL adaptor proteins: networks for physiological and pathological signaling

被引:210
|
作者
Birge, Raymond B. [1 ]
Kalodimos, Charalampos [2 ]
Inagaki, Fuyuhiko [3 ]
Tanaka, Shinya [4 ]
机构
[1] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Biochem & Mol Biol, Newark, NJ 07103 USA
[2] Rutgers State Univ, Dept Chem Chem Biol & Biomed Engn, Piscataway, NJ 08854 USA
[3] Hokkaido Univ, Grad Sch Pharmaceut Sci, Dept Biol Struct, Kita Ku, Sapporo, Hokkaido 0010021, Japan
[4] Hokkaido Univ, Sch Med, Div Med, Dept Pathol,Kita Ku, Sapporo, Hokkaido 0608638, Japan
关键词
FOCAL ADHESION KINASE; TERMINAL SH3 DOMAIN; NUCLEOTIDE EXCHANGE FACTOR; SRC FAMILY KINASES; DEPENDENT TYROSINE PHOSPHORYLATION; GROWTH-FACTOR RECEPTOR; PROGRAMMED CELL-DEATH; V-CRK; C-CRK; ENDOTHELIAL-CELLS;
D O I
10.1186/1478-811X-7-13
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Crk adaptor proteins (Crk and CrkL) constitute an integral part of a network of essential signal transduction pathways in humans and other organisms that act as major convergence points in tyrosine kinase signaling. Crk proteins integrate signals from a wide variety of sources, including growth factors, extracellular matrix molecules, bacterial pathogens, and apoptotic cells. Mounting evidence indicates that dysregulation of Crk proteins is associated with human diseases, including cancer and susceptibility to pathogen infections. Recent structural work has identified new and unusual insights into the regulation of Crk proteins, providing a rationale for how Crk can sense diverse signals and produce a myriad of biological responses.
引用
收藏
页数:23
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