| Literature DB >> 24064037 |
Dmitri Kharitidi1, Sanaz Manteghi2, Arnim Pause3.
Abstract
Protein tyrosine phosphatases (PTPs) are key enzymes in the regulation of cellular homeostasis and signaling pathways. Strikingly, not all PTPs bear enzymatic activity. A considerable fraction of PTPs are enzymatically inactive and are known as pseudophosphatases. Despite the lack of activity they execute pivotal roles in development, cell biology and human disease. The present review is focused on the methods used to identify pseudophosphatases, their targets, and physiological roles. We present a strategy for detailed enzymatic analysis of inactive PTPs, regulation of inactive PTP domains and identification of binding partners. Furthermore, we provide a detailed overview of human pseudophosphatases and discuss their regulation of cellular processes and functions in human pathologies.Entities:
Keywords: PTP; Phosphatase assays; Phosphotyrosine binding domain; Pseudophosphatase; Substrate-trapping
Mesh:
Substances:
Year: 2013 PMID: 24064037 DOI: 10.1016/j.ymeth.2013.09.009
Source DB: PubMed Journal: Methods ISSN: 1046-2023 Impact factor: 3.608