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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >A Functional Proteomics Approach Links The Ubiquitin-related Modifier Urm1 To A Trna Modification Pathway
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A Functional Proteomics Approach Links The Ubiquitin-related Modifier Urm1 To A Trna Modification Pathway

机译:功能蛋白质组学方法将泛素相关修饰子Urm1链接到Trna修饰途径

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摘要

Urm1 is a highly conserved ubiquitin-related modifier of unknown function. A reduction of cellular Urm1 levels causes severe cytokinesis defects in HeLa cells, resulting in the accumulation of enlarged multinucleated cells. To understand the underlying mechanism, we applied a functional proteomics approach and discovered an enzymatic activity that links Urm1 to a tRNA modification pathway. Unlike ubiquitin (Ub) and many Ub-like modifiers, which are commonly conjugated to proteinaceous targets, Urm1 is activated by an unusual mechanism to yield a thiocarboxylate intermediate that serves as sulfur donor in tRNA thiolation reactions. This mechanism is reminiscent of that used by prokaryotic sulfur carriers and thus defines the evolutionary link between ancient Ub progenitors and the eukaryotic Ub/Ub-like modification systems.
机译:Urm1是功能未知的高度保守的泛素相关修饰因子。细胞Urm1水平的降低会导致HeLa细胞发生严重的胞质分裂缺陷,从而导致扩大的多核细胞积聚。为了了解潜在的机制,我们应用了功能蛋白质组学方法,并发现了将Urm1连接到tRNA修饰途径的酶活性。与泛素(Ub)和通常与蛋白质靶标共轭的许多Ub-like修饰剂不同,Urm1被一种不寻常的机制激活,从而生成硫代羧酸盐中间体,在tRNA硫醇化反应中用作硫供体。这种机制使人联想到原核硫载体所使用的机制,因此定义了古代Ub祖细胞与真核Ub / Ub样修饰系统之间的进化联系。

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