Catic André, Collins Cal, Church George M, Ploegh Hidde L
Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.
Bioinformatics. 2004 Dec 12;20(18):3302-7. doi: 10.1093/bioinformatics/bth407. Epub 2004 Jul 15.
The conjugation of ubiquitin to target molecules involves several enzymatic steps. Little is known about the specificity of ubiquitination. How E3 ligases select their substrate and which lysines are targeted for ubiquitin conjugation is largely an enigma. The object of this study is to identify preferred ubiquitination sites. Genetic approaches to study this question have proven difficult, because of the redundancy of ligases and the lack of strictly required motifs. However, a better understanding of acceptor site selection could help to predict ubiquitination sites and clarify yet unsolved structure-function relationships of the transfer reaction.
In an effort to define preferences for ubiquitination, we systematically analyzed structure and sequence of 135 known ubiquitination sites in 95 proteins in Saccharomyces cerevisiae. The results show clear structural preferences for ubiquitin ligation to target proteins, and compartment-specific amino acid patterns in close proximity to the modified side chain.
泛素与靶分子的缀合涉及多个酶促步骤。人们对泛素化的特异性了解甚少。E3连接酶如何选择其底物以及哪些赖氨酸被靶向用于泛素缀合在很大程度上仍是一个谜。本研究的目的是确定优先的泛素化位点。由于连接酶的冗余性和缺乏严格必需的基序,用遗传方法研究这个问题已被证明很困难。然而,更好地理解受体位点选择有助于预测泛素化位点,并阐明尚未解决的转移反应的结构-功能关系。
为了确定泛素化的偏好,我们系统地分析了酿酒酵母中95种蛋白质中135个已知泛素化位点的结构和序列。结果显示了泛素与靶蛋白连接的明显结构偏好,以及与修饰侧链紧邻的特定区域的氨基酸模式。