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An in cellulo-derived structure of PAK4 in complex with its inhibitor Inka1

机译:PAK4的纤维素衍生结构及其抑制剂Inka1

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摘要

PAK4 is a metazoan-specific kinase acting downstream of Cdc42. Here we describe the structure of human PAK4 in complex with Inka1, a potent endogenous kinase inhibitor. Using single mammalian cells containing crystals 50 mm in length, we have determined the in cellulo crystal structure at 2.95 angstrom resolution, which reveals the details of how the PAK4 catalytic domain binds cellular ATP and the Inka1 inhibitor. The crystal lattice consists only of PAK4-PAK4 contacts, which form a hexagonal array with channels of 80 angstrom in diameter that run the length of the crystal. The crystal accommodates a variety of other proteins when fused to the kinase inhibitor. Inka1-GFP was used to monitor the process crystal formation in living cells. Similar derivatives of Inka1 will allow us to study the effects of PAK4 inhibition in cells and model organisms, to allow better validation of therapeutic agents targeting PAK4.
机译:PAK4是在Cdc42下游起作用的后生动物特异性激酶。在这里,我们描述了与有效的内源性激酶抑制剂Inka1结合的人PAK4的结构。使用包含50毫米长的晶体的单个哺乳动物细胞,我们确定了2.95埃分辨率的细胞内晶体结构,这揭示了PAK4催化域如何结合细胞ATP和Inka1抑制剂的细节。晶格仅由PAK4-PAK4触点组成,它们形成一个六边形阵列,其直径为80埃的通道沿着晶体的长度延伸。当与激酶抑制剂融合时,晶体可容纳多种其他蛋白质。 Inka1-GFP用于监测活细胞中过程晶体的形成。 Inka1的类似衍生物将使我们能够研究PAK4在细胞和模型生物中的抑制作用,以便更好地验证靶向PAK4的治疗剂。

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