Everett John K, Tejero Roberto, Murthy Sarath B K, Acton Thomas B, Aramini James M, Baran Michael C, Benach Jordi, Cort John R, Eletsky Alexander, Forouhar Farhad, Guan Rongjin, Kuzin Alexandre P, Lee Hsiau-Wei, Liu Gaohua, Mani Rajeswari, Mao Binchen, Mills Jeffrey L, Montelione Alexander F, Pederson Kari, Powers Robert, Ramelot Theresa, Rossi Paolo, Seetharaman Jayaraman, Snyder David, Swapna G V T, Vorobiev Sergey M, Wu Yibing, Xiao Rong, Yang Yunhuang, Arrowsmith Cheryl H, Hunt John F, Kennedy Michael A, Prestegard James H, Szyperski Thomas, Tong Liang, Montelione Gaetano T
Center for Advanced Biotechnology and Medicine, Department of Molecular Biology and Biochemistry, and Northeast Structural Genomics Consortium, Rutgers, the State University of New Jersey, Piscataway, New Jersey, 08854, USA.
Departamento De Química Física, Universidad De Valencia, Valencia, Spain.
Protein Sci. 2016 Jan;25(1):30-45. doi: 10.1002/pro.2774. Epub 2015 Sep 22.
We have developed an online NMR / X-ray Structure Pair Data Repository. The NIGMS Protein Structure Initiative (PSI) has provided many valuable reagents, 3D structures, and technologies for structural biology. The Northeast Structural Genomics Consortium was one of several PSI centers. NESG used both X-ray crystallography and NMR spectroscopy for protein structure determination. A key goal of the PSI was to provide experimental structures for at least one representative of each of hundreds of targeted protein domain families. In some cases, structures for identical (or nearly identical) constructs were determined by both NMR and X-ray crystallography. NMR spectroscopy and X-ray diffraction data for 41 of these "NMR / X-ray" structure pairs determined using conventional triple-resonance NMR methods with extensive sidechain resonance assignments have been organized in an online NMR / X-ray Structure Pair Data Repository. In addition, several NMR data sets for perdeuterated, methyl-protonated protein samples are included in this repository. As an example of the utility of this repository, these data were used to revisit questions about the precision and accuracy of protein NMR structures first outlined by Levy and coworkers several years ago (Andrec et al., Proteins 2007;69:449-465). These results demonstrate that the agreement between NMR and X-ray crystal structures is improved using modern methods of protein NMR spectroscopy. The NMR / X-ray Structure Pair Data Repository will provide a valuable resource for new computational NMR methods development.
我们开发了一个在线核磁共振/ X射线结构对数据存储库。美国国立综合医学科学研究所(NIGMS)的蛋白质结构计划(PSI)为结构生物学提供了许多有价值的试剂、三维结构和技术。东北结构基因组学联盟是PSI的几个中心之一。NESG使用X射线晶体学和核磁共振光谱法来确定蛋白质结构。PSI的一个关键目标是为数百个靶向蛋白质结构域家族中的每一个家族至少提供一个代表性的实验结构。在某些情况下,相同(或几乎相同)构建体的结构通过核磁共振和X射线晶体学两种方法确定。使用传统的三共振核磁共振方法并进行广泛的侧链共振归属确定的41对这些“核磁共振/ X射线”结构对的核磁共振光谱和X射线衍射数据已整理在一个在线核磁共振/ X射线结构对数据存储库中。此外,该存储库还包含了一些全氘代、甲基质子化蛋白质样品的核磁共振数据集。作为该存储库实用性的一个例子,这些数据被用于重新审视几年前Levy及其同事首次提出的关于蛋白质核磁共振结构的精度和准确性的问题(Andrec等人,《蛋白质》,2007年;69:449 - 465)。这些结果表明,使用现代蛋白质核磁共振光谱方法,核磁共振和X射线晶体结构之间的一致性得到了提高。核磁共振/ X射线结构对数据存储库将为新的计算核磁共振方法开发提供宝贵的资源。