THE PH DOMAIN - A COMMON PIECE IN THE STRUCTURAL PATCHWORK OF SIGNALING PROTEINS

被引:511
作者
MUSACCHIO, A
GIBSON, T
RICE, P
THOMPSON, J
SARASTE, M
机构
[1] European Molecular Biology Laboratory, D-69012 Heidelberg
关键词
D O I
10.1016/0968-0004(93)90071-T
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 'pleckstrin homology' domain is an approximately 100-residue protein module that has recently been added to the domain catalogue of signalling proteins. For this review we have made an extensive database search using a profile search method, and found a number of additional proteins that may contain PH domains. The PH domain is present in many kinases, isoforms of phospholipase C, GTPases, GTPase-activating proteins and nucleotide-exchange factors, including such proteins as Vav, Dbl and Bcr, and there are two PH domains in a guanine-nucleotide releasing factor of Ras. Many PH-domain-containing proteins interact with GTP-binding proteins. We have also identified a PH domain in beta-adrenergic receptor kinase exactly in the region that has already been shown to be involved in binding to the beta and gamma subunits of a heterotrimeric G protein. This suggests that PH domains may be involved in interactions with GTP-binding proteins.
引用
收藏
页码:343 / 348
页数:6
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