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 h...
The human genome encodes about 285 proteins that contain at least one annotated pleckstrin homology ...
Background:Pleckstrin homology (PH) domains are found in many proteins involved in signal transducti...
Pleckstrin homology (PH) domains are presumed to bind phosphoinositides (PIPs) but only few specific...
The 'pleckstrin homology' domain is an approximately 100-residue protein module that has recently be...
A diverse array of molecules involved in signal transduction have recently been recognised as contai...
AbstractThe initial reports on pleckstrin homology (PH) domains almost 20years ago described them as...
AbstractPleckstrin homology (PH) domains are discrete structural modules present in numerous protein...
THE pleckstrin homology (PH) domain is a new protein module of around 100 amino acids found in sever...
The pleckstrin homology [PH] domain is a structural fold found in more than 250 proteins making it t...
AbstractPleckstrin homology (PH) domains are 100–120 amino acid protein modules best known for their...
The 'pleckstrin homology' or PH domain is a 100-residue protein module. It is present in many kinase...
The 'pleckstrin homology' or PH domain is a 100-residue protein module. It is present in many kinase...
AbstractSince their discovery almost 10 years ago pleckstrin homology (PH) domains have been identif...
Some of the pleckstrin homology (PH) domains are shown to bind bg-subunits of a G-protein. In this p...
The human genome encodes about 285 proteins that contain at least one annotated pleckstrin homology ...
The human genome encodes about 285 proteins that contain at least one annotated pleckstrin homology ...
Background:Pleckstrin homology (PH) domains are found in many proteins involved in signal transducti...
Pleckstrin homology (PH) domains are presumed to bind phosphoinositides (PIPs) but only few specific...
The 'pleckstrin homology' domain is an approximately 100-residue protein module that has recently be...
A diverse array of molecules involved in signal transduction have recently been recognised as contai...
AbstractThe initial reports on pleckstrin homology (PH) domains almost 20years ago described them as...
AbstractPleckstrin homology (PH) domains are discrete structural modules present in numerous protein...
THE pleckstrin homology (PH) domain is a new protein module of around 100 amino acids found in sever...
The pleckstrin homology [PH] domain is a structural fold found in more than 250 proteins making it t...
AbstractPleckstrin homology (PH) domains are 100–120 amino acid protein modules best known for their...
The 'pleckstrin homology' or PH domain is a 100-residue protein module. It is present in many kinase...
The 'pleckstrin homology' or PH domain is a 100-residue protein module. It is present in many kinase...
AbstractSince their discovery almost 10 years ago pleckstrin homology (PH) domains have been identif...
Some of the pleckstrin homology (PH) domains are shown to bind bg-subunits of a G-protein. In this p...
The human genome encodes about 285 proteins that contain at least one annotated pleckstrin homology ...
The human genome encodes about 285 proteins that contain at least one annotated pleckstrin homology ...
Background:Pleckstrin homology (PH) domains are found in many proteins involved in signal transducti...
Pleckstrin homology (PH) domains are presumed to bind phosphoinositides (PIPs) but only few specific...