利用LatPack对任意晶格蛋白模型中的蛋白样序列进行分类。

Hfsp Journal Pub Date : 2008-12-01 Epub Date: 2008-11-26 DOI:10.2976/1.3027681
Martin Mann, Daniel Maticzka, Rhodri Saunders, Rolf Backofen
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引用次数: 17

摘要

了解蛋白质的三维天然结构对于确定其化学性质和功能至关重要。然而,用实验方法来确定结构是非常昂贵和耗时的。折叠模拟和结构预测算法等计算方法更快、更便宜,但缺乏一致的准确性。这目前限制了广泛的计算研究抽象的蛋白质模型。因此,由模型引起的简化不能否定科学价值,这一点至关重要。关键是使用完全定义的蛋白质样序列。在这种情况下,抽象模型可以用来研究重要的生物学问题。在这里,我们提出了一个程序来生成和分类蛋白质样序列数据集。我们的LatPack工具和方法一般适用于任意晶格蛋白质模型。鉴定是基于热力学动力学特征,并结合顺序组装的蛋白质通过解决共翻译折叠。我们在广泛使用的无限制3d立方hp模型中演示了该方法。结果序列集是该模型显示所需的蛋白质样特性的第一个大型数据集。我们的数据工具是免费提供的,可用于研究蛋白质相关问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Classifying proteinlike sequences in arbitrary lattice protein models using LatPack.

Knowledge of a protein's three-dimensional native structure is vital in determining its chemical properties and functionality. However, experimental methods to determine structure are very costly and time-consuming. Computational approaches such as folding simulations and structure prediction algorithms are quicker and cheaper but lack consistent accuracy. This currently restricts extensive computational studies to abstract protein models. It is thus essential that simplifications induced by the models do not negate scientific value. Key to this is the use of thoroughly defined proteinlike sequences. In such cases abstract models can allow for the investigation of important biological questions. Here, we present a procedure to generate and classify proteinlike sequence data sets. Our LatPack tools and the approach in general are applicable to arbitrary lattice protein models. Identification is based on thermodynamic kinetic features and incorporates the sequential assembly of proteins by addressing cotranslational folding. We demonstrate the approach in the widely used unrestricted 3D-cubic HP-model. The resulting sequence set is the first large data set for this model exhibiting the proteinlike properties required. Our data tools are freely available and can be used to investigate protein-related problems.

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Hfsp Journal
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