Boston College, Department of Chemistry, Merkert Chemistry Center, Chestnut Hill, MA 02467, USA.
J Mol Graph Model. 2013 Mar;40:48-53. doi: 10.1016/j.jmgm.2012.12.012. Epub 2013 Jan 5.
The biological functions of many enzymes are often coupled with significant conformational changes. The end states of these conformational changes can often be determined by X-ray crystallography. These X-ray structures are snapshots of the two extreme conformations in which the macromolecule exists, but the dynamic movements between the states are not easily visualized in a two-dimensional illustration. Here we have developed a new method to visualize macromolecular motions called a ViewMotions Rainbow diagram. These diagrams show the initial and final states overlaid along with approximately 30 intermediate structures calculated by linear interpolation of the backbone coordinates of the initial and final states. This group of structures is then spectrally colored from the initial structure in blue to the final structure in red. ViewMotions Rainbow diagrams provide the reader with a much easier way to understand the macromolecular motions using a single two-dimensional illustration. Since producing these diagrams requires a number of different software packages, we have setup the ViewMotions Web Server (http://viewmotions.bc.edu) to automatically generate these diagrams from two Protein Data Bank files or from the Database of Macromolecular Movements (http://molmovdb.org).
许多酶的生物学功能通常与显著的构象变化相关联。这些构象变化的终态通常可以通过 X 射线晶体学来确定。这些 X 射线结构是大分子存在的两个极端构象的静态快照,但在二维图中不容易直观地看到状态之间的动态运动。在这里,我们开发了一种称为 ViewMotions Rainbow 图的新方法来可视化大分子运动。这些图显示了初始状态和最终状态的叠加,以及通过初始和最终状态的骨架坐标线性插值计算得到的大约 30 个中间结构。然后,这组结构从初始结构的蓝色到最终结构的红色进行光谱着色。ViewMotions Rainbow 图为读者提供了一种更简单的方法,可以通过单个二维图来理解大分子运动。由于生成这些图需要许多不同的软件包,因此我们建立了 ViewMotions Web 服务器(http://viewmotions.bc.edu),可以从两个蛋白质数据库文件或大分子运动数据库(http://molmovdb.org)自动生成这些图。