Department of Supramolecular Biology, Graduate School of Nanobioscience, Yokohama City University, Tsurumi-ku, Yokohama 230-0045, Japan.
Proteins. 2012 Nov;80(11):2592-600. doi: 10.1002/prot.24143. Epub 2012 Jul 31.
We have developed a method to place an EF-lobe in a coordinate system that recognizes the similarity of its two EF-hand domains as well as their relationship by a pseudo-two fold axis, z. The x-axis connects the center of mass, calculated from α-carbons of helices E1 and F1, with the center of mass of E2 and F2. The resulting coordinate system is intrinsic to each EF-lobe and requires no comparison with other EF-lobes. It has provided an intuitive and informative way to compare EF-lobes and especially those changes associated with calcium and/or target binding. We analyzed the EF-lobes of calmodulin and of other subfamilies with four EF-hands. We have rationalized a complex pattern of changes of conformation associated with calcium coordination and effector binding as observed in different subfamilies of EF-hand proteins.
我们开发了一种将 EF 环置于坐标系中的方法,该坐标系通过伪二折叠轴 z 识别其两个 EF 手结构域的相似性及其关系。x 轴连接从 E1 和 F1 螺旋的α-碳原子计算出的质心,与 E2 和 F2 的质心相连。由此产生的坐标系是每个 EF 环所固有的,无需与其他 EF 环进行比较。它为比较 EF 环,特别是与钙和/或靶标结合相关的变化提供了一种直观且信息丰富的方法。我们分析了钙调蛋白和其他具有四个 EF 手的亚家族的 EF 环。我们已经合理化了与钙配位和效应物结合相关的构象变化的复杂模式,如在不同的 EF 手蛋白亚家族中观察到的那样。