Kline A D, Braun W, Wüthrich K
Institut für Molekularbiologie und Biophysik, Eidgenössische Technische Hochschule-Hönggerberg, Zürich, Switzerland.
J Mol Biol. 1988 Dec 5;204(3):675-724. doi: 10.1016/0022-2836(88)90364-6.
The complete three-dimensional structure of the alpha-amylase inhibitor Tendamistat in aqueous solution was determined by 1H nuclear magnetic resonance and distance geometry calculations using the program DISMAN. Compared to an earlier, preliminary determination of the polypeptide backbone conformation, stereo-specific assignments were obtained for 41 of the 89 prochiral groups in the protein, and a much more extensive set of experimental constraints was collected, including 842 distance constraints from nuclear Overhauser effects and over 100 supplementary constraints from spin-spin coupling constants and the identification of intramolecular hydrogen bonds. The complete protein molecule, including the amino acid side-chains is characterized by a group of nine structures corresponding to the results of the nine DISMAN calculations with minimal residual error functions. The average of the pairwise minimal root-mean-square distances among these nine structures is 0.85 A for the polypeptide backbone, and 1.52 A for all the heavy atoms. The procedures used for the structure determination are described and a detailed analysis is presented of correlations between the experimental input data and the precision of the structure determination.
通过使用DISMAN程序进行的1H核磁共振和距离几何计算,确定了水溶液中α-淀粉酶抑制剂Tendamistat的完整三维结构。与早期对多肽主链构象的初步测定相比,该蛋白质中89个前手性基团中的41个获得了立体特异性归属,并且收集了更为广泛的一组实验约束条件,包括来自核Overhauser效应的842个距离约束以及来自自旋-自旋耦合常数和分子内氢键识别的100多个补充约束。完整的蛋白质分子,包括氨基酸侧链,由一组九个结构表征,这些结构对应于具有最小残差函数的九次DISMAN计算结果。这九个结构之间成对最小均方根距离的平均值,多肽主链为0.85埃,所有重原子为1.52埃。描述了用于结构测定的程序,并对实验输入数据与结构测定精度之间的相关性进行了详细分析。