Department of Chemistry, Seoul National University, Seoul 151-747, Republic of Korea.
J Comput Chem. 2012 Sep 15;33(24):1927-35. doi: 10.1002/jcc.23024. Epub 2012 May 30.
A homology model builder using simple restraining potentials based on spline-interpolated quadratic functions is developed and interfaced with CHARMM package. The continuity and stability of the potential function were validated, and the parameters were optimized using the CASP7 targets. The performance of the model builder was benchmarked to the Modeller program using the template-based modeling targets in CASP9. The benchmark results show that, while our builder yields the structures with slightly lower packing, backbone, and template modeling scores, our models show much better protein-like scores in terms of normalized discrete optimized protein energy, dipolar distance-scaled finite-ideal gas reference, Molprobity clash, Ramachandran appearance Z-score, and rotamer Z-score. As our model builder is interfaced with CHARMM, it is advantageous to directly use other CHARMM functionality and energy functions to refine the model structures or to use the models for other computational studies using CHARMM.
开发了一种基于样条插值二次函数的简单约束势同源建模程序,并与 CHARMM 软件包进行了接口。验证了势函数的连续性和稳定性,并使用 CASP7 目标优化了参数。使用 CASP9 中的基于模板的建模目标对模型构建器的性能与 Modeller 程序进行了基准测试。基准测试结果表明,虽然我们的构建器生成的结构具有略低的堆积、主链和模板建模评分,但在归一化离散优化蛋白能、偶极距离缩放有限理想气体参考、Molprobity 碰撞、Ramachandran 外观 Z 分数和构象 Z 分数方面,我们的模型表现出更好的蛋白样评分。由于我们的模型构建器与 CHARMM 进行了接口,因此直接使用其他 CHARMM 功能和能量函数来优化模型结构或使用 CHARMM 进行其他计算研究具有优势。