This chapter describes the Ras and Rap I interaction with AF-6 effector target. The chapter presents a spectrum of investigative approaches that served to demonstrate specific protein interactions among the Ras/Rapl GTPases and their potential effector molecule AF-6 in vivo and in vitro. The Rap types of small GTPases are members of the Ras superfamily and are the molecules that show the most identity with the oncogenic Ras proteins. Whereas the interaction of activated Ras proteins with their downstream effectors Raf, Ral guanine nucleotide dissociation stimulator (RalGDS), and phosphatidylinositol 3-kinase (PI3K) leads to a fairly defined picture, the role of Rapl is as yet poorly understood. The two-hybrid analysis and the investigation ...
AbstractRas plays the role of a molecular switch in many cellular signalling pathways. The Raf-kinas...
Ras and Rap proteins are closely related small GTPases. Whereas Ras is known for its role in cell pr...
AbstractThe structure of the complex of Ras with the Ras-binding domain of its effector RalGDS (RGS-...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
To identify proteins that bind to the Ras-related protein R-ras we performed a yeast two-hybrid cDNA...
RaplA (Krev-l) is a member of the Ras superfamily of small GTP-binding proteins and has highest homo...
Small GTPases of the Ras family are major players of signal transduction in eukaryotic cells. They r...
Although Ras and Rap1 share interaction with common candidate effector proteins, Rap1 lacks the tran...
Although Ras and Rap1 share interaction with common candidate effector proteins, Rap1 lacks the tran...
The AF-6 protein is a multidomain protein that contains two potential Ras-binding domains within its...
AbstractRas plays the role of a molecular switch in many cellular signalling pathways. The Raf-kinas...
Small GTPases of the Ras family are major players of signal transduction in eukaryotic cells. They r...
AbstractRas plays the role of a molecular switch in many cellular signalling pathways. The Raf-kinas...
Ras and Rap proteins are closely related small GTPases. Whereas Ras is known for its role in cell pr...
AbstractThe structure of the complex of Ras with the Ras-binding domain of its effector RalGDS (RGS-...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
Cellular signaling downstream of Ras is highly diversified and may involve many different effector m...
To identify proteins that bind to the Ras-related protein R-ras we performed a yeast two-hybrid cDNA...
RaplA (Krev-l) is a member of the Ras superfamily of small GTP-binding proteins and has highest homo...
Small GTPases of the Ras family are major players of signal transduction in eukaryotic cells. They r...
Although Ras and Rap1 share interaction with common candidate effector proteins, Rap1 lacks the tran...
Although Ras and Rap1 share interaction with common candidate effector proteins, Rap1 lacks the tran...
The AF-6 protein is a multidomain protein that contains two potential Ras-binding domains within its...
AbstractRas plays the role of a molecular switch in many cellular signalling pathways. The Raf-kinas...
Small GTPases of the Ras family are major players of signal transduction in eukaryotic cells. They r...
AbstractRas plays the role of a molecular switch in many cellular signalling pathways. The Raf-kinas...
Ras and Rap proteins are closely related small GTPases. Whereas Ras is known for its role in cell pr...
AbstractThe structure of the complex of Ras with the Ras-binding domain of its effector RalGDS (RGS-...