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Determination of Mutation Pattern in Human Androgen Receptor by Means of Amino-Acid Pair Predictability

机译:氨基酸对可预测性确定人雄激素受体的突变型

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The mutation trend and pattern in protein are currently studied directly using amino acid sequence, however, it would be more efficient if the amino acid sequence is transferred into other domains through quantification because sophisticated mathematical tools can be applied to a numeric sequence. In this study, we apply the amino-acid pair predictability to quantifying the human androgen receptor with its 215 missense point mutations to analyze which amino-acid pairs are sensitive to mutations. The results show that 94.88% mutations occurred at the unpredictable amino-acid pairs, 79% mutations targeted at one or two original amino-acid pairs whose actual frequency is larger than predicted frequency and 63.26% mutations lead to one or two mutated amino-acid pairs with their actual frequency smaller than predicted one.
机译:目前直接使用氨基酸序列研究蛋白质中的突变趋势和模式,但是,如果将氨基酸序列通过定量转移到其他域中会更有效,因为可以将复杂的数学工具应用于数字序列。在这项研究中,我们将氨基酸对的可预测性用于量化其215个错义点突变的人类雄激素受体,从而分析哪些氨基酸对突变敏感。结果表明,94.88%的突变发生在不可预测的氨基酸对上,79%的突变针对一个或两个原始氨基酸对,其实际频率大于预测的频率,63.26%的突变导致一个或两个突变的氨基酸对,其实际频率小于预测的频率。

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