| Literature DB >> 15489887 |
Charles E Ducker1, Erin M Stettler, Kevin J French, John J Upson, Charles D Smith.
Abstract
Protein palmitoyltransferases (PATs) represent an exciting new target for anticancer drug design due to their pivotal roles in the subcellular localization of a number of oncogenes. We show that the Huntingtin interacting protein 14 (HIP14) is a PAT with a preference for the farnesyl-dependent palmitoylation motif found in H- and N-RAS. Characterization of HIP14 in mouse cells has revealed that it has the ability to induce colony formation in cell culture, anchorage-independent growth, and tumors in mice. Activity of the enzyme and its ability to transform cells is dependent on critical residues in the active site of the enzyme.Entities:
Mesh:
Substances:
Year: 2004 PMID: 15489887 PMCID: PMC2908390 DOI: 10.1038/sj.onc.1208171
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867