A New Approach for Sequence Analysis: Illustrating an Expanded Bioinformatics View through Exploring Properties of the Prestin Protein

K. Dempsey, Benjamin Currall, R. Hallworth, H. Ali
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引用次数: 11

Abstract

Understanding the structure-function relationship of proteins offers the key to biological processes, and can offer knowledge for better investigation of matters with widespread impact, such as pathological disease and drug intervention. This relationship is dictated at the simplest level by the primary protein sequence. Since useful structures and functions are conserved within biology, a sequence with known structure-function relationship can be compared to related sequences to aid in novel structure-function prediction. Sequence analysis provides a means for suggesting evolutionary relationships, and inferring structural or functional similarity. It is crucial to consider these parameters while comparing sequences as they influence both the algorithms used and the implications of the results. For example, proteins that are closely related on an evolutionary time scale may have very similar structure, but entirely different functions. In contrast, proteins which have undergone convergent evolution may have dissimilar primary structure, but perform similar functions. This chapter details how the aspects of evolution, structure, and function can be taken into account when performing sequence analysis, and proposes an expansion on traditional approaches resulting in direct improvement of said analysis. This model is applied to a case study in the prestin protein and shows that the proposed approach provides a better understanding of input and output and can improve the performance of sequence analysis by means of motif detection software. Kathryn Dempsey University of Nebraska at Omaha, USA & University of Nebraska Medical Center, USA Benjamin Currall Creighton University, USA Richard Hallworth Creighton University, USA Hesham Ali University of Nebraska at Omaha, USA & University of Nebraska Medical Center, USA DOI: 10.4018/978-1-4666-3604-0.ch079
序列分析的新方法:通过探索Prestin蛋白的特性来阐述扩展的生物信息学观点
了解蛋白质的结构-功能关系是了解生物过程的关键,可以为更好地研究具有广泛影响的问题提供知识,例如病理疾病和药物干预。这种关系在最简单的水平上由初级蛋白质序列决定。由于有用的结构和功能在生物学中是保守的,具有已知结构-功能关系的序列可以与相关序列进行比较,以帮助新的结构-功能预测。序列分析提供了提示进化关系和推断结构或功能相似性的手段。在比较序列时考虑这些参数是至关重要的,因为它们会影响所使用的算法和结果的含义。例如,在进化时间尺度上密切相关的蛋白质可能具有非常相似的结构,但功能完全不同。相反,经历趋同进化的蛋白质可能具有不同的初级结构,但具有相似的功能。本章详细介绍了在进行序列分析时如何考虑进化、结构和功能方面,并提出了对传统方法的扩展,从而直接改进所述分析。该模型应用于prestin蛋白的案例研究,结果表明该方法可以更好地理解输入和输出,并可以通过基序检测软件提高序列分析的性能。Kathryn Dempsey内布拉斯加州大学奥马哈分校和内布拉斯加州大学医学中心,美国本杰明·科瑞尔·克雷顿大学,美国理查德·霍尔沃思·克雷顿大学,美国内布拉斯加州大学奥马哈分校和内布拉斯加州大学医学中心,美国DOI: 10.4018/978-1-4666-3604-0.ch079
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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