Membrane Targeting by Pleckstrin Homology Domains
- 1 January 2004
- book chapter
- Published by Springer Nature
- Vol. 282, 49-88
- https://doi.org/10.1007/978-3-642-18805-3_3
Abstract
Pleckstrin homology (PH) domains are small modular domains that occur once, or occasionally several times, in a large variety of signalling proteins. In a number of instances, PH domains act to target their host protein to the cytosolic face of cellular membranes through an ability to associate with phosphoinositides. In this review,we discuss recent advances in our understanding of PH domain function. In particular we describe the structural aspects of how PH domains have evolved to bind various phosphoinositides, how PH domains regulate phosphoinositide-mediated association to plasma and internals membranes, and finally raise the issue of PH domains in protein:protein interactions and the allosteric regulation of their host protein.Keywords
This publication has 103 references indexed in Scilit:
- Structural basis for the selective activation of Rho GTPases by Dbl exchange factorsNature Structural & Molecular Biology, 2002
- Tumor Suppressor PTEN Mediates Sensing of Chemoattractant GradientsCell, 2002
- RACK1, a Protein Kinase C Scaffolding Protein, Interacts with the PH Domain of p120GAPBiochemical and Biophysical Research Communications, 2001
- Structure of the Enabled/VASP Homology 1 Domain–Peptide Complex: A Key Component in the Spatial Control of Actin AssemblyCell, 1999
- Insulin-dependent translocation of ARNO to the plasma membrane of adipocytes requires phosphatidylinositol 3-kinaseCurrent Biology, 1998
- The solution structure of the pleckstrin homology domain of mouse son-of-sevenless 1 (msos1)Journal of Molecular Biology, 1997
- Automated NOESY interpretation with ambiguous distance restraints: the refined NMR solution structure of the pleckstrin homology domain from β-spectrin 1 1Edited by P. E. WrightJournal of Molecular Biology, 1997
- Molecular Cloning and Characterization of a New Member of the RAC Protein Kinase Family: Association of the Pleckstrin Homology Domain of 3 Types of RAC Protein Kinase with Protein Kinase C Subspecies and βγ Subunits of G ProteinsBiochemical and Biophysical Research Communications, 1995
- Binding of Pleckstrin Homology Domains to WD40/β-Transducin Repeat Containing Segments of the Protein Product of the Lis-1 GeneBiochemical and Biophysical Research Communications, 1995
- The Pleckstrin Homology Domain of RAC Protein Kinase Associates with the Regulatory Domain of Protein Kinase C ζBiochemical and Biophysical Research Communications, 1994