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2016 ◽  
Vol 94 (5) ◽  
Author(s):  
Jacopo Iacovacci ◽  
Lucas Lacasa

2015 ◽  
Vol 4 (1) ◽  
pp. 127-139 ◽  
Author(s):  
Colin Campbell ◽  
Katriona Shea ◽  
Suann Yang ◽  
Réka Albert

2001 ◽  
Vol 114 (16) ◽  
pp. 2903-2910 ◽  
Author(s):  
Margaret A. Lawlor ◽  
Dario R. Alessi

The serine/threonine protein kinase PKB (also known as Akt) is thought to be a key mediator of signal transduction processes. The identification of PKB substrates and the role PKB phosphorylation plays in regulating these molecules have been a major focus of research in recent years. A recently developed motif-profile scoring algorithm that can be used to scan the genome for potential PKB substrates is therefore a useful tool, although additional considerations, such as the evolutionary conservation of the phosphorylation site, must also be taken into account. Recent evidence indicates that PKB plays a key role in cancer progression by stimulating cell proliferation and inhibiting apoptosis and is also probably a key mediator of insulin signalling. These findings indicate that PKB is likely to be a hot drug target for the treatment of cancer, diabetes and stroke. There are, however, a number of pitfalls of methodologies currently employed to study PKB function, and therefore caution should be used in interpretation of such experiments.


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