Redfern Oliver C, Dessailly Benoit, Orengo Christine A
Department of Structural and Molecular Biology, University College London, London WC1E 6BT, United Kingdom.
Curr Opin Struct Biol. 2008 Jun;18(3):394-402. doi: 10.1016/j.sbi.2008.05.007.
Advances in protein structure determination, led by the structural genomics initiatives have increased the proportion of novel folds deposited in the Protein Data Bank. However, these structures are often not accompanied by functional annotations with experimental confirmation. In this review, we reassess the meaning of structural novelty and examine its relevance to the complexity of the structure-function paradigm. Recent advances in the prediction of protein function from structure are discussed, as well as new sequence-based methods for partitioning large, diverse superfamilies into biologically meaningful clusters. Obtaining structural data for these functionally coherent groups of proteins will allow us to better understand the relationship between structure and function.
由结构基因组学计划引领的蛋白质结构测定技术的进步,增加了蛋白质数据库中新型折叠结构的比例。然而,这些结构往往没有经过实验证实的功能注释。在本综述中,我们重新评估了结构新颖性的含义,并探讨了其与结构 - 功能范式复杂性的相关性。我们讨论了从结构预测蛋白质功能的最新进展,以及基于序列的新方法,这些方法可将庞大且多样的超家族划分为具有生物学意义的簇。获取这些功能相关蛋白质组的结构数据将使我们能够更好地理解结构与功能之间的关系。