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There's More to Death Than Life: Noncatalytic Functions in Kinase and Pseudokinase Signaling

Overview
Journal J Biol Chem
Specialty Biochemistry
Date 2021 Apr 25
PMID 33895136
Citations 27
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Abstract

Protein kinases are present in all domains of life and play diverse roles in cellular signaling. Whereas the impact of substrate phosphorylation by protein kinases has long been appreciated, it is becoming increasingly clear that protein kinases also play other, noncatalytic, functions. Here, we review recent developments in understanding the noncatalytic functions of protein kinases. Many noncatalytic activities are best exemplified by protein kinases that are devoid of enzymatic activity altogether-known as pseudokinases. These dead proteins illustrate that, beyond conventional notions of kinase function, catalytic activity can be dispensable for biological function. Through key examples we illustrate diverse mechanisms of noncatalytic kinase activity: as allosteric modulators; protein-based switches; scaffolds for complex assembly; and as competitive inhibitors in signaling pathways. In common, these noncatalytic mechanisms exploit the nature of the protein kinase fold as a versatile protein-protein interaction module. Many examples are also intrinsically linked to the ability of the protein kinase to switch between multiple states, a function shared with catalytic protein kinases. Finally, we consider the contemporary landscape of small molecules to modulate noncatalytic functions of protein kinases, which, although challenging, has significant potential given the scope of noncatalytic protein kinase function in health and disease.

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References
1.
Jacobsen A, Murphy J . The secret life of kinases: insights into non-catalytic signalling functions from pseudokinases. Biochem Soc Trans. 2017; 45(3):665-681. DOI: 10.1042/BST20160331. View

2.
Caenepeel S, Charydczak G, Sudarsanam S, Hunter T, Manning G . The mouse kinome: discovery and comparative genomics of all mouse protein kinases. Proc Natl Acad Sci U S A. 2004; 101(32):11707-12. PMC: 511041. DOI: 10.1073/pnas.0306880101. View

3.
Khamrui S, Ung P, Secor C, Schlessinger A, Lazarus M . High-Resolution Structure and Inhibition of the Schizophrenia-Linked Pseudokinase ULK4. J Am Chem Soc. 2019; 142(1):33-37. PMC: 7261596. DOI: 10.1021/jacs.9b10458. View

4.
Samson A, Zhang Y, Geoghegan N, Gavin X, Davies K, Mlodzianoski M . MLKL trafficking and accumulation at the plasma membrane control the kinetics and threshold for necroptosis. Nat Commun. 2020; 11(1):3151. PMC: 7305196. DOI: 10.1038/s41467-020-16887-1. View

5.
Ha B, Boggon T . The crystal structure of pseudokinase PEAK1 (Sugen kinase 269) reveals an unusual catalytic cleft and a novel mode of kinase fold dimerization. J Biol Chem. 2017; 293(5):1642-1650. PMC: 5798295. DOI: 10.1074/jbc.RA117.000751. View