Eswar Narayanan, Webb Ben, Marti-Renom Marc A, Madhusudhan M S, Eramian David, Shen Min-Yi, Pieper Ursula, Sali Andrej
University of California at San Francisco San Francisco, California.
Curr Protoc Bioinformatics. 2006 Oct;Chapter 5:Unit-5.6. doi: 10.1002/0471250953.bi0506s15.
Functional characterization of a protein sequence is one of the most frequent problems in biology. This task is usually facilitated by accurate three-dimensional (3-D) structure of the studied protein. In the absence of an experimentally determined structure, comparative or homology modeling can sometimes provide a useful 3-D model for a protein that is related to at least one known protein structure. Comparative modeling predicts the 3-D structure of a given protein sequence (target) based primarily on its alignment to one or more proteins of known structure (templates). The prediction process consists of fold assignment, target-template alignment, model building, and model evaluation. This unit describes how to calculate comparative models using the program MODELLER and discusses all four steps of comparative modeling, frequently observed errors, and some applications. Modeling lactate dehydrogenase from Trichomonas vaginalis (TvLDH) is described as an example. The download and installation of the MODELLER software is also described.
蛋白质序列的功能表征是生物学中最常见的问题之一。这项任务通常借助所研究蛋白质精确的三维(3-D)结构来推进。在缺乏实验确定的结构时,比较建模或同源建模有时可为与至少一种已知蛋白质结构相关的蛋白质提供有用的3-D模型。比较建模主要基于给定蛋白质序列(目标序列)与一种或多种已知结构蛋白质(模板)的比对来预测其3-D结构。预测过程包括折叠识别、目标-模板比对、模型构建和模型评估。本单元描述了如何使用MODELLER程序计算比较模型,并讨论了比较建模的所有四个步骤、常见错误及一些应用。以阴道毛滴虫乳酸脱氢酶(TvLDH)的建模为例进行了说明。还介绍了MODELLER软件的下载与安装。