Pemodelan蛋白dengan同源性建模

Noer Komari, Samsul Hadi, Eko Suhartono
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引用次数: 7

摘要

蛋白质的三维结构是了解蛋白质性质和功能的必要条件。用实验室设备测定蛋白质结构是相当复杂和昂贵的。预测蛋白质三维结构的一种替代方法。其中一种计算机方法是同调建模。同源建模是使用SWISS-MODEL服务器完成的。将在3D结构中建模的蛋白质是在RCSB PDB数据库中尚未具有结构的蛋白质。蛋白质序列从UniProt数据库中获取,代码为A0A0B6VWS2。结果表明,共选择了两种模型,即PDB代码模板1q0e的模型1和PDB代码模板3gtv的模型2。序列比对和模型可视化结果表明,模型1和模型2是一致的。模型1对Ramachandran地块的评价和评价的有利面积为97.36%,MolProbity评分为0.79,QMEAN值为1.13。model -1是一个很好的三维蛋白质结构模型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pemodelan Protein dengan Homology Modeling menggunakan SWISS-MODEL
The three-dimensional (3D) structure of proteins is necessary to understand the properties and functions of proteins. Determining protein structure by laboratory equipment is quite complicated and expensive. An alternative method to predict the 3D structure of proteins in the in silico method. One of the in silico methods is homology modeling. Homology modeling is done using the SWISS-MODEL server. Proteins that will be modeled in the 3D structure are proteins that do not yet have a structure in the RCSB PDB database. Protein sequences were obtained from the UniProt database with code A0A0B6VWS2. The results showed that there were two models selected, namely model-1 with the PDB code template 1q0e and model-2 with the PDB code template 3gtv. The results of sequence alignment and model visualization show that model-1 and model-2 are identical. The evaluation and assessment of model-1 on the Ramachandran Plot have a Favored area of ??97.36%, a MolProbity score of 0.79, and a QMEAN value is 1.13. Model-1 is a good 3D protein structure model.
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