Department of Bioinformatics, School of Life Sciences, Bharathidasan University, Tiruchirappalli 620024, India.
Genomics Proteomics Bioinformatics. 2013 Apr;11(2):114-21. doi: 10.1016/j.gpb.2012.11.005. Epub 2013 Mar 21.
For the past few decades, intensive studies have been carried out in an attempt to understand how the amino acid sequences of proteins encode their three dimensional structures to perform their specific functions. In order to understand the sequence-structure relationship of proteins, several sub-sequence search studies in non-redundant sequence-structure databases have been undertaken which have given some fruitful clues. In our earlier work, we analyzed a set of 3124 non-redundant protein sequences from the Protein Data Bank (PDB) and retrieved 30 identical octapeptides having different secondary structures. These octapeptides were characterized by using different computational procedures. This prompted us to explore the presence of octapeptides with reverse sequences and to analyze whether these octapeptides would adopt similar structures as that of their parent octapeptides. Our identical reverse octapeptide search resulted in the finding of eight octapeptide pairs (octapeptide and reverse octapeptide) with similar secondary structure and 23 octapeptide pairs with different secondary structures. In the present work, the geometrical and biophysical characteristics of identical reverse octapeptides were explored and compared with unrelated octapeptide pairs by using various computational tools. We thus conclude that proteins containing identical reverse octapeptides are not very abundant and residues in the octapeptide pairs do not contribute to the stability of the protein. Furthermore, compared to unrelated octapeptides, identical reverse octapeptides do not show certain biophysical and geometrical properties.
在过去的几十年中,人们进行了大量的研究,试图了解蛋白质的氨基酸序列如何编码其三维结构以执行其特定功能。为了理解蛋白质的序列-结构关系,已经在非冗余序列-结构数据库中进行了几项子序列搜索研究,这些研究提供了一些有价值的线索。在我们之前的工作中,我们分析了来自蛋白质数据库 (PDB) 的一组 3124 个非冗余蛋白质序列,并检索到了 30 个具有不同二级结构的相同八肽。这些八肽通过使用不同的计算程序进行了表征。这促使我们探索具有反向序列的八肽的存在,并分析这些八肽是否会采用与其母体八肽相似的结构。我们的相同反向八肽搜索结果发现了八对具有相似二级结构的八肽(八肽和反向八肽)和 23 对具有不同二级结构的八肽。在目前的工作中,通过使用各种计算工具,探索了相同反向八肽的几何和生物物理特性,并将其与不相关的八肽对进行了比较。因此,我们得出结论,含有相同反向八肽的蛋白质并不是很丰富,并且八肽对中的残基不会对蛋白质的稳定性做出贡献。此外,与不相关的八肽相比,相同的反向八肽不表现出某些生物物理和几何特性。