The dead phosphatases society: a review of the emerging roles of pseudophosphatases
- PMID: 32484316
- DOI: 10.1111/febs.15431
The dead phosphatases society: a review of the emerging roles of pseudophosphatases
Abstract
Phosphatases are a diverse family of enzymes, comprising at least 10 distinct protein folds. Like most other enzyme families, many have sequence variations that predict an impairment or loss of catalytic activity classifying them as pseudophosphatases. Research on pseudoenzymes is an emerging area of interest, with new biological functions repurposed from catalytically active relatives. Here, we provide an overview of the pseudophosphatases identified to date in all major phosphatase families. We will highlight the degeneration of the various catalytic sequence motifs and discuss the challenges associated with the experimental determination of catalytic inactivity. We will also summarize the role of pseudophosphatases in various diseases and discuss the major challenges and future directions in this field.
Keywords: dephosphorylation; phosphatase; pseudoenzymes; pseudophosphatase.
© 2020 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.
References
-
- Lim WA & Pawson T (2010) Phosphotyrosine signaling: evolving a new cellular communication system. Cell 142, 661-667.
-
- Murphy JM, Farhan H & Eyers PA (2017) Bio-Zombie: the rise of pseudoenzymes in biology. Biochem Soc Trans 45, 537-544.
-
- Ribeiro AJM, Das S, Dawson N, Zaru R, Orchard S, Thornton JM, Orengo C, Zeqiraj E, Murphy JM & Eyers PA (2019) Emerging concepts in pseudoenzyme classification, evolution, and signaling. Sci Signal 12, eaat9797.
-
- Reiterer V, Eyers PA & Farhan H (2014) Day of the dead: pseudokinases and pseudophosphatases in physiology and disease. Trends Cell Biol 24, 489-505.
-
- Black MH, Osinski A, Gradowski M, Servage KA, Pawłowski K, Tomchick DR & Tagliabracci VS (2019) Bacterial pseudokinase catalyzes protein polyglutamylation to inhibit the SidE-family ubiquitin ligases. Science 364, 787-792.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
