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Bioinformatic Screening of Autoimmune Disease Genes and Protein Structure Prediction with FAMS for Drug Discovery

机译:利用FAMS进行自身免疫性疾病基因的生物信息学筛选和蛋白质结构预测,以发现药物

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摘要

Autoimmune diseases are often intractable because their causes are unknown. Identifying which genes contribute to these diseases may allow us to understand the pathogenesis, but it is difficult to determine which genes contribute to disease. Recently, epigenetic information has been considered to activate/deactivate disease-related genes. Thus, it may also be useful to study epigenetic information that differs between healthy controls and patients with autoimmune disease. Among several types of epigenetic information, promoter methylation is believed to be one of the most important factors. Here, we propose that principal component analysis is useful to identify specific gene promoters that are differently methylated between the normal healthy controls and patients with autoimmune disease. Full Automatic Modeling System (FAMS) was used to predict the three-dimensional structures of selected proteins and successfully inferred relatively confident structures. Several possibilities of the application to the drug discovery based on obtained structures are discussed.
机译:自身免疫性疾病通常难以治疗,因为其病因尚不清楚。鉴定哪些基因导致这些疾病可能使我们了解发病机理,但是很难确定哪些基因导致疾病。最近,已经考虑了表观遗传信息来激活/失活与疾病相关的基因。因此,研究健康对照与自身免疫性疾病患者之间的表观遗传信息也可能有用。在几种表观遗传信息中,启动子甲基化被认为是最重要的因素之一。在这里,我们建议主成分分析可用于识别在正常健康对照和自身免疫性疾病患者之间甲基化程度不同的特定基因启动子。全自动建模系统(FAMS)用于预测所选蛋白质的三维结构,并成功推断出相对可信的结构。讨论了基于获得的结构应用于药物发现的几种可能性。

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