Inhibitors of Protein: Geranylgeranyl Transferases
- Authors: Farid El Oualid, Gijs A. van der Marel, Mark Overhand3
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View Affiliations Hide Affiliations3 Netherlands Cancer Institute, Division of Cell Biology, 1066 CX Amsterdam, The Netherlands, Netherlands
- Source: Frontiers in Medicinal Chemistry: Volume 5 , pp 167-233
- Publication Date: December 2010
- Language: English
Inhibitors of Protein: Geranylgeranyl Transferases, Page 1 of 1
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The enzyme protein:geranylgeranyl transferase-1 (PGGT-1 or GGTase-I) catalyzes the geranylgeranylation of cysteine residues near the C-termini of a variety of proteins, including most monomeric GTP binding precursor proteins belonging to the Rho, Rac and Rap subfamilies. These proteins are involved in signaling pathways controlling important processes such as cell differentiation and growth. In the framework of the development of therapeutics against disorders associated with aberrant cell proliferation, the interference with these signal transduction cascades has been a major focus of investigation. For instance, PGGT-1 inhibitors have shown promise in the treatment of cancer, smooth muscle hyperplasia as well as parasitic infections, such as malaria. In this chapter, we discuss the structural and mechanistic aspects of the protein:geranylgeranyl transferases and their importance with respect to the terpene metabolism. In view of the latter, several terpene based proteomic probes have been developed and applied. An extensive summary of reported inhibitors of PGGT-1, classified as natural products, peptide substrate (Ca1a2L box), terpene substrate (geranylgeranyl pyrophosphate) and others, is presented. The few known inhibitors of the other geranylgeranylating enzyme, protein:geranylgeranyl transferase-2 (PGGT-2) also known as Rab geranylgeranyl transferase are also included.
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