Holm L, Sander C
European Bioinformatics Institute, European Molecular Biology Laboratory, Hinxton Hall, Cambridge CB10 1SD, UK.
Science. 1996 Aug 2;273(5275):595-603. doi: 10.1126/science.273.5275.595.
The comparison of the three-dimensional shapes of protein molecules poses a complex algorithmic problem. Its solution provides biologists with computational tools to organize the rapidly growing set of thousands of known protein shapes, to identify new types of protein architecture, and to discover unexpected evolutionary relations, reaching back billions of years, between protein molecules. Protein shape comparison also improves tools for identifying gene functions in genome databases by defining the essential sequence-structure features of a protein family. Finally, an exhaustive all-on-all shape comparison provides a map of physical attractor regions in the abstract shape space of proteins, with implications for the processes of protein folding and evolution.
蛋白质分子三维形状的比较带来了一个复杂的算法问题。其解决方案为生物学家提供了计算工具,用于整理迅速增长的数千种已知蛋白质形状的集合,识别新型蛋白质结构,并发现蛋白质分子之间可追溯到数十亿年前的意外进化关系。蛋白质形状比较还通过定义蛋白质家族的基本序列-结构特征,改进了在基因组数据库中识别基因功能的工具。最后,详尽的全对全形状比较提供了蛋白质抽象形状空间中物理吸引子区域的图谱,这对蛋白质折叠和进化过程具有启示意义。