Dolinsky Todd J, Nielsen Jens E, McCammon J Andrew, Baker Nathan A
Department of Biochemistry and Molecular Biophysics, Center for Computational Biology, Washington University in St Louis, 700 S. Euclid Avenue, Campus Box 8036, St Louis, MO 63110, USA.
Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W665-7. doi: 10.1093/nar/gkh381.
Continuum solvation models, such as Poisson-Boltzmann and Generalized Born methods, have become increasingly popular tools for investigating the influence of electrostatics on biomolecular structure, energetics and dynamics. However, the use of such methods requires accurate and complete structural data as well as force field parameters such as atomic charges and radii. Unfortunately, the limiting step in continuum electrostatics calculations is often the addition of missing atomic coordinates to molecular structures from the Protein Data Bank and the assignment of parameters to biomolecular structures. To address this problem, we have developed the PDB2PQR web service (http://agave.wustl.edu/pdb2pqr/). This server automates many of the common tasks of preparing structures for continuum electrostatics calculations, including adding a limited number of missing heavy atoms to biomolecular structures, estimating titration states and protonating biomolecules in a manner consistent with favorable hydrogen bonding, assigning charge and radius parameters from a variety of force fields, and finally generating 'PQR' output compatible with several popular computational biology packages. This service is intended to facilitate the setup and execution of electrostatics calculations for both experts and non-experts and thereby broaden the accessibility to the biological community of continuum electrostatics analyses of biomolecular systems.
连续介质溶剂化模型,如泊松-玻尔兹曼方法和广义玻恩方法,已日益成为研究静电对生物分子结构、能量学和动力学影响的常用工具。然而,使用这些方法需要准确完整的结构数据以及诸如原子电荷和半径等力场参数。不幸的是,连续介质静电计算中的限制步骤通常是向来自蛋白质数据库的分子结构中添加缺失的原子坐标以及为生物分子结构分配参数。为了解决这个问题,我们开发了PDB2PQR网络服务(http://agave.wustl.edu/pdb2pqr/)。该服务器自动执行许多为连续介质静电计算准备结构的常见任务,包括向生物分子结构中添加有限数量的缺失重原子、估计滴定状态并以符合有利氢键的方式对生物分子进行质子化、从各种力场分配电荷和半径参数,最后生成与几个流行的计算生物学软件包兼容的“PQR”输出。此服务旨在促进专家和非专家进行静电计算的设置和执行,从而扩大生物分子系统连续介质静电分析在生物界的可及性。