Ponting C P, Phillips C, Davies K E, Blake D J
University of Oxford, Fibrinolysis Research Unit, UK.
Bioessays. 1997 Jun;19(6):469-79. doi: 10.1002/bies.950190606.
PDZ (also called DHR or GLGF) domains are found in diverse membrane-associated proteins including members of the MAGUK family of guanylate kinase homologues, several protein phosphatases and kinases, neuronal nitric oxide synthase, and several dystrophin-associated proteins, collectively known as syntrophins. Many PDZ domain-containing proteins appear to be localised to highly specialised submembranous sites, suggesting their participation in cellular junction formation, receptor or channel clustering, and intracellular signalling events. PDZ domains of several MAGUKs interact with the C-terminal polypeptides of a subset of NMDA receptor subunits and/or with Shaker-type K+ channels. Other PDZ domains have been shown to bind similar ligands of other transmembrane receptors. Recently, the crystal structures of PDZ domains, with and without ligand, have been determined. These demonstrate the mode of ligand-binding and the structural bases for sequence conservation among diverse PDZ domains.
PDZ(也称为DHR或GLGF)结构域存在于多种与膜相关的蛋白质中,包括鸟苷酸激酶同源物MAGUK家族的成员、几种蛋白磷酸酶和激酶、神经元型一氧化氮合酶以及几种与肌营养不良蛋白相关的蛋白质,统称为肌萎缩蛋白相关蛋白。许多含有PDZ结构域的蛋白质似乎定位于高度特化的膜下位点,这表明它们参与细胞连接形成、受体或通道聚集以及细胞内信号转导事件。几种MAGUK的PDZ结构域与NMDA受体亚基子集的C末端多肽和/或与Shaker型钾通道相互作用。其他PDZ结构域已被证明可结合其他跨膜受体的类似配体。最近,已确定了有配体和无配体的PDZ结构域的晶体结构。这些结构展示了配体结合模式以及不同PDZ结构域间序列保守性的结构基础。