Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA.
Antioxid Redox Signal. 2011 Jul 1;15(1):135-46. doi: 10.1089/ars.2010.3561. Epub 2011 Apr 14.
Cysteine (Cys) residues serve many functions, such as catalysis, stabilization of protein structure through disulfides, metal binding, and regulation of protein function. Cys residues are also subject to numerous post-translational modifications. In recent years, various computational tools aiming at classifying and predicting different functional categories of Cys have been developed, particularly for structural and catalytic Cys. On the other hand, given complexity of the subject, bioinformatics approaches have been less successful for the investigation of regulatory Cys sites. In this review, we introduce different functional categories of Cys residues. For each category, an overview of state-of-the-art bioinformatics methods and tools is provided, along with examples of successful applications and potential limitations associated with each approach. Finally, we discuss Cys-based redox switches, which modify the view of distinct functional categories of Cys in proteins.
半胱氨酸(Cys)残基具有多种功能,如催化、通过二硫键稳定蛋白质结构、金属结合和调节蛋白质功能。Cys 残基还受到许多翻译后修饰的影响。近年来,已经开发了各种旨在对不同功能类别 Cys 进行分类和预测的计算工具,特别是针对结构和催化 Cys。另一方面,由于该主题的复杂性,生物信息学方法在研究调节 Cys 位点方面的效果较差。在这篇综述中,我们介绍了 Cys 残基的不同功能类别。对于每种类别,我们提供了最新的生物信息学方法和工具的概述,以及每种方法的成功应用和潜在局限性的示例。最后,我们讨论了基于 Cys 的氧化还原开关,它改变了蛋白质中不同功能类别 Cys 的观点。