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iDNA-Protdis: Identifying DNA-Binding Proteins by Incorporating Amino Acid Distance-Pairs and Reduced Alphabet Profile into the General Pseudo Amino Acid Composition

机译:iDNA-Prot dis:通过将氨基酸距离对和降低的字母特征整合到一般的伪氨基酸组成中来鉴定DNA结合蛋白

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摘要

Playing crucial roles in various cellular processes, such as recognition of specific nucleotide sequences, regulation of transcription, and regulation of gene expression, DNA-binding proteins are essential ingredients for both eukaryotic and prokaryotic proteomes. With the avalanche of protein sequences generated in the postgenomic age, it is a critical challenge to develop automated methods for accurate and rapidly identifying DNA-binding proteins based on their sequence information alone. Here, a novel predictor, called “iDNA-Prot|dis”, was established by incorporating the amino acid distance-pair coupling information and the amino acid reduced alphabet profile into the general pseudo amino acid composition (PseAAC) vector. The former can capture the characteristics of DNA-binding proteins so as to enhance its prediction quality, while the latter can reduce the dimension of PseAAC vector so as to speed up its prediction process. It was observed by the rigorous jackknife and independent dataset tests that the new predictor outperformed the existing predictors for the same purpose. As a user-friendly web-server, iDNA-Prot|dis is accessible to the public at . Moreover, for the convenience of the vast majority of experimental scientists, a step-by-step protocol guide is provided on how to use the web-server to get their desired results without the need to follow the complicated mathematic equations that are presented in this paper just for the integrity of its developing process. It is anticipated that the iDNA-Prot|dis predictor may become a useful high throughput tool for large-scale analysis of DNA-binding proteins, or at the very least, play a complementary role to the existing predictors in this regard.
机译:DNA结合蛋白在各种细胞过程中发挥着至关重要的作用,例如识别特定的核苷酸序列,调节转录和调节基因表达,是真核和原核蛋白质组中必不可少的成分。随着在后基因组时代产生的大量蛋白质序列,开发仅基于其序列信息即可准确,快速地鉴定DNA结合蛋白的自动化方法是一项严峻的挑战。在此,通过将氨基酸距离对偶联信息和氨基酸减少的字母分布图整合到一般的伪氨基酸组成(PseAAC)载体中,建立了称为“ iDNA-Prot”的新型预测因子。前者可以捕获DNA结合蛋白的特征,从而提高其预测质量,而后者可以减小PseAAC载体的大小,从而加快其预测过程。通过严格的折刀和独立的数据集测试发现,出于相同的目的,新的预测变量优于现有的预测变量。作为用户友好的Web服务器,iDNA-Prot | dis可以通过公众访问。此外,为了方便绝大多数实验科学家,还提供了有关如何使用网络服务器获得所需结果的分步协议指南,而无需遵循本教程中介绍的复杂数学方程式。本文仅出于其开发过程的完整性。可以预期,iDNA-Prot预测子可能成为用于大规模分析DNA结合蛋白的有用的高通量工具,或者至少在这方面起与现有预测子的互补作用。

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