Barrera Exequiel E, Pantano Sergio, Zonta Francesco
Instituto de Histología y Embriología (IHEM) - Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), CC56, Universidad Nacional de Cuyo (UNCuyo), Mendoza, Argentina.
Biomolecular Simulations Group, Institut Pasteur de Montevideo, Mataojo 2020, CP 11400 Montevideo, Uruguay.
Data Brief. 2021 Apr 30;36:107109. doi: 10.1016/j.dib.2021.107109. eCollection 2021 Jun.
This dataset contains a collection of molecular dynamics (MD) simulations of polyglutamine (polyQ) and glutamine-rich (Q-rich) peptides in the multi-microsecond timescale. Primary data from coarse-grained simulations performed using the SIRAH force field has been processed to provide fully atomistic coordinates. The dataset encloses MD trajectories of polyQs of 4 (Q4), 11 (Q11), and 36 (Q36) amino acids long. In the case of Q11, simulations in presence of Q5 and QEQQQ peptides, which modulate aggregation, are also included. The dataset also comprises MD trajectories of the gliadin related p31-43 peptide, and Insulin's C-peptide at pH=7 and pH=3.2, which constitute examples of Q-rich and Q-poor aggregating peptides. The dataset grants molecular insights on the role of glutamines in spontaneous and unbiased ab-initio aggregation of a series of peptides using a homogeneous set of simulations [1]. The trajectory files are provided in Protein Data Bank (PDB) format containing the Cartesian coordinates of all heavy atoms in the aggregating peptides. Further analyses of the trajectories can be performed directly using any molecular visualization/analysis software suites.
该数据集包含多微秒时间尺度下聚谷氨酰胺(polyQ)和富含谷氨酰胺(Q-rich)肽的分子动力学(MD)模拟集合。使用SIRAH力场进行的粗粒度模拟的原始数据已被处理以提供全原子坐标。该数据集包含长度为4个(Q4)、11个(Q11)和36个(Q36)氨基酸的聚谷氨酰胺的MD轨迹。对于Q11,还包括在调节聚集的Q5和QEQQQ肽存在下的模拟。该数据集还包括麦醇溶蛋白相关的p31 - 43肽以及pH = 7和pH = 3.2时胰岛素C肽的MD轨迹,它们分别是富含Q和贫Q聚集肽的实例。该数据集通过一组均匀的模拟,对谷氨酰胺在一系列肽的自发和无偏从头聚集过程中的作用提供了分子层面的见解[1]。轨迹文件以蛋白质数据库(PDB)格式提供,包含聚集肽中所有重原子的笛卡尔坐标。可以直接使用任何分子可视化/分析软件套件对轨迹进行进一步分析。