From Src Homology domains to other signaling modules: proposal of the 'protein recognition code'

被引:192
作者
Sudol, M [1 ]
机构
[1] CUNY Mt Sinai Sch Med, Dept Biochem, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
protein modules; protein motifs; genetic code; phosphotyrosine; polyproline;
D O I
10.1038/sj.onc.1202182
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The study of oncogenes has illuminated many aspects of cellular signaling. The delineation and characterization of protein modules exemplified by Src Homology domains has revolutionized our understanding of the molecular events underlying signal transduction pathways. Several well characterized intracellular modules which mediate protein-protein interactions, namely SH2, SH3, PH, PTB, EH, PDZ, EVH1 and WW domains, are directly involved in the multitude of membrane, cytoplasmic and nuclear processes in multicellular and/or unicellular organisms. The modular character of these protein domains and their cognate motifs, the universality of their molecular function, their widespread occurrence, and the specificity as well as the degeneracy of their interactions have prompted us to propose the concept of the 'protein recognition code'. By a parallel analogy to the universal genetic code, we propose here that there will be a finite set of precise rules to govern and predict protein-protein interactions mediated by modules. Several rules of the 'protein recognition code' have already emerged.
引用
收藏
页码:1469 / 1474
页数:6
相关论文
共 64 条
  • [51] A SINGLE-POINT MUTATION SWITCHES THE SPECIFICITY OF GROUP-III SRC HOMOLOGY (SH) 2 DOMAINS TO THAT OF GROUP-I SH2 DOMAINS
    SONGYANG, Z
    GISH, G
    MBAMALU, G
    PAWSON, T
    CANTLEY, LC
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (44) : 26029 - 26032
  • [52] Recognition of unique carboxyl-terminal motifs by distinct PDZ domains
    Songyang, Z
    Fanning, AS
    Fu, C
    Xu, J
    Marfatia, SM
    Chishti, AH
    Crompton, A
    Chan, AC
    Anderson, JM
    Cantley, LC
    [J]. SCIENCE, 1997, 275 (5296) : 73 - 77
  • [53] Songyang Zhou, 1995, Trends in Biochemical Sciences, V20, P470, DOI 10.1016/S0968-0004(00)89103-3
  • [54] SEQUENCE SIMILARITY OF PHOSPHOLIPASE-C WITH THE NON-CATALYTIC REGION OF SRC
    STAHL, ML
    FERENZ, CR
    KELLEHER, KL
    KRIZ, RW
    KNOPF, JL
    [J]. NATURE, 1988, 332 (6161) : 269 - 272
  • [55] STICKER NL, 1997, NAT BIOTECHNOL, V15, P336
  • [56] The WW module competes with the SH3 domain?
    Sudol, M
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1996, 21 (05) : 161 - 163
  • [57] Structure and function of the WW domain
    Sudol, M
    [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1996, 65 (1-2) : 113 - 132
  • [58] A CONSERVED AMINO-TERMINAL SHC DOMAIN BINDS TO PHOSPHOTYROSINE MOTIFS IN ACTIVATED RECEPTORS AND PHOSPHOPEPTIDES
    VANDERGEER, P
    WILEY, S
    LAI, VKM
    OLIVIER, JP
    GISH, GD
    STEPHENS, R
    KAPLAN, D
    SHOELSON, S
    PAWSON, T
    [J]. CURRENT BIOLOGY, 1995, 5 (04) : 404 - 412
  • [59] THE PTB DOMAIN - A NEW-PROTEIN MODULE IMPLICATED IN SIGNAL-TRANSDUCTION
    VANDERGEER, P
    PAWSON, T
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (07) : 277 - 280
  • [60] p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin
    Watanabe, N
    Madaule, P
    Reid, T
    Ishizaki, T
    Watanabe, G
    Kakizuka, A
    Saito, Y
    Nakao, K
    Jockusch, BM
    Narumiya, S
    [J]. EMBO JOURNAL, 1997, 16 (11) : 3044 - 3056