1Centre for Systems Biology, Samuel Lunenfeld Research Institute, Toronto, Ontario M5G 1X5, Canada.
Sci Signal. 2010 Mar 2;3(111):pe8. doi: 10.1126/scisignal.3111pe8.
Protein kinases regulate a plethora of diverse cellular functions. Their highly controlled activation is subject to an equally diverse repertoire of regulatory mechanisms. Pseudokinases, a class of proteins that possess a structurally related protein kinase domain that lacks phospho-transfer function, are emerging as critical yet mysterious regulators of other protein kinases. A new structural and functional analysis of the pseudokinase STRAD provides insight into the mechanism by which it allosterically regulates the catalytic function of the protein kinase LKB1 and hints at an evolution from a classical kinase-substrate relationship.
蛋白激酶调节着多种多样的细胞功能。它们的高度受控激活受到同样多样化的调控机制的影响。假激酶是一类具有结构相关的蛋白激酶结构域但缺乏磷酸转移功能的蛋白质,它们作为其他蛋白激酶的关键而神秘的调节剂而崭露头角。对假激酶 STRAD 的新的结构和功能分析提供了关于其变构调节蛋白激酶 LKB1 的催化功能的机制的深入了解,并暗示了从经典的激酶-底物关系的进化。