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蛋白质类泛素化修饰的系统研究:SUMOsp 2.0位点特异性预测工具的开发。

Systematic study of protein sumoylation: Development of a site-specific predictor of SUMOsp 2.0.

作者信息

Ren Jian, Gao Xinjiao, Jin Changjiang, Zhu Mei, Wang Xiwei, Shaw Andrew, Wen Longping, Yao Xuebiao, Xue Yu

机构信息

Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, Hefei, Anhui, P. R. China.

Department of Physiology and Cancer Biology Program, Morehouse School of Medicine, Atlanta, GA, USA.

出版信息

Proteomics. 2009 Jun;9(12):3409-3412. doi: 10.1002/pmic.200800646. Epub 2009 Jun 5.

DOI:10.1002/pmic.200800646
PMID:29658196
Abstract

Protein sumoylation is an important reversible post-translational modification on proteins, and orchestrates a variety of cellular processes. Recently, computational prediction of sumoylation sites has attracted much attention for its cost-efficiency and power in genomic data mining. In this work, we developed SUMOsp 2.0, an accurate computing program with an improved group-based phosphorylation scoring algorithm. Our analysis demonstrated that SUMOsp 2.0 has greater prediction accuracy than SUMOsp 1.0 and other existing tools, with a sensitivity of 88.17% and a specificity of 92.69% under the medium threshold. Previously, several large-scale experiments have identified a list of potential sumoylated substrates in Saccharomyces cerevisiae and Homo sapiens; however, the exact sumoylation sites in most of these proteins remain elusive. We have predicted potential sumoylation sites in these proteins using SUMOsp 2.0, which provides a great resource for researchers and an outline for further mechanistic studies of sumoylation in cellular plasticity and dynamics. The online service and local packages of SUMOsp 2.0 are freely available at: http://sumosp.biocuckoo.org/.

摘要

蛋白质SUMO化是一种重要的蛋白质可逆翻译后修饰,它调控着多种细胞过程。最近,SUMO化位点的计算预测因其在基因组数据挖掘中的成本效益和强大功能而备受关注。在这项工作中,我们开发了SUMOsp 2.0,这是一个具有改进的基于基团的磷酸化评分算法的精确计算程序。我们的分析表明,SUMOsp 2.0比SUMOsp 1.0和其他现有工具具有更高的预测准确性,在中等阈值下灵敏度为88.17%,特异性为92.69%。此前,一些大规模实验已经确定了酿酒酵母和人类中一系列潜在的SUMO化底物;然而,这些蛋白质中大多数的确切SUMO化位点仍然不清楚。我们使用SUMOsp 2.0预测了这些蛋白质中的潜在SUMO化位点,这为研究人员提供了丰富的资源,并为进一步研究SUMO化在细胞可塑性和动力学中的机制提供了一个框架。SUMOsp 2.0的在线服务和本地程序包可在以下网址免费获取:http://sumosp.biocuckoo.org/ 。

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