Computational and functional analysis of the putative SH2 domain in Janus Kinases

被引:33
作者
Kampa, D
Burnside, J [1 ]
机构
[1] Univ Delaware, Dept Anim & Food Sci, Newark, DE 19717 USA
[2] Univ Delaware, Dept Chem & Biochem, Newark, DE 19717 USA
关键词
Janus tyrosine kinase; SH2; domain; structure determination; web-based computational analysis;
D O I
10.1006/bbrc.2000.3757
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
Src homology 2 (SH2) domains interact in a highly specific manner with phosphorylated tyrosine residues on other signaling molecules. Protein tyrosine kinases (PTK) frequently contain SH2 domains, which often control signaling specificity. The Janus Kinases (JAKs) are a family of PTKs involved in signal transduction]pathways mediated by various cytokines. Initial characterization of JAKs showed no identifiable SH2 domain. However, we have found substantial evidence supporting the existence of an SH2 domain in JAKs through the use of various web-based computational analysis programs. Predictive secondary and tertiary structures recognize an SH2 domain in JAKs. In addition, a three-dimensional homology model was constructed using the SH2 domains of Src tyrosine kinase and Syp tyrosine phosphatase as templates. These results, in conjunction with preliminary binding studies showing interactions with tyrosine phosphorylated proteins in activated splenocytes, suggest a functional role for this domain in JAKs. (C) 2000 Academic Press.
引用
收藏
页码:175 / 182
页数:8
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