Phosphorylation-specific prolyl isomerization: is there an underlying theme?

G Wulf, G Finn, F Suizu, KP Lu - Nature cell biology, 2005 - nature.com
G Wulf, G Finn, F Suizu, KP Lu
Nature cell biology, 2005nature.com
The prolyl isomerase Pin1 is a conserved enzyme that is intimately involved in diverse
biological processes and pathological conditions such as cancer and Alzheimer's disease.
By catalysing cis–trans interconversion of certain motifs containing phosphorylated serine or
threonine residues followed by a proline residue (pSer/Thr-Pro), Pin1 can have profound
effects on phosphorylation signalling. The structural and functional differences that result
from cis–trans isomerization of specific pSer/Thr-Pro motifs probably underlie most, if not all …
Abstract
The prolyl isomerase Pin1 is a conserved enzyme that is intimately involved in diverse biological processes and pathological conditions such as cancer and Alzheimer's disease. By catalysing cis–trans interconversion of certain motifs containing phosphorylated serine or threonine residues followed by a proline residue (pSer/Thr-Pro), Pin1 can have profound effects on phosphorylation signalling. The structural and functional differences that result from cis–trans isomerization of specific pSer/Thr-Pro motifs probably underlie most, if not all, Pin1-dependent actions. Phosphorylation-dependent prolyl isomerization by Pin1 remains a unique mode for the modulation of signal transduction. Here, we provide an overview of the plethora of regulatory events that involve this unique enzyme, with a particular focus on oncogenic signalling and neurodegeneration.
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