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A computational approach for mining cholesterol and their potential target against GPCR seven helices based on spectral clustering and fuzzy c-means algorithms

机译:基于光谱聚类和模糊C型算法的采矿胆固醇及其对GPCR七螺旋的潜在目标的计算方法

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摘要

In modern biology, GPCRs occupy a solitary crossroad and it signifies as important families of membrane receptors. In human body, all intracellular communications and cell signaling can take place with the knowledge of GPCR protein. Cholesterol is a vital sterol that is requisite for cell development and differentiation in mammalian cells. Modulating the function of several membrane proteins membrane cholesterol plays a significant role. Among these proteins, a particular cholesterol binding motif is reported to which the membrane cholesterol binds and modulates their movement. This consensus motif is either seen as CRAC and CARC, which correspond to any amino acid between one and five residues. Therefore, the recentwork is focused on human GPCR transporters to identify the allocation of this motif in all seven helices of GPCR family and provide a harmony signature motif for an individual helix. A computational approach based on Spectral Clustering using Fuzzy c-Means has been experimented to obtain heterogeneous type of sequence for cholesterol from GPCR super family. From the obtained result, it is seen that excluding olfactory family in our dataset we found perfect matching of cholesterol motif with Transmembrane helices of GPCR family which can be further extended to other membrane proteins.
机译:在现代生物学中,GPCR占据孤独的十字路口,它表示为膜受体的重要家族。在人体中,所有细胞内通信和细胞信号都可以通过GPCR蛋白的知识进行。胆固醇是一种重要的甾醇,是哺乳动物细胞中细胞开发和分化的必要条件。调节几种膜蛋白胆固醇的功能起着重要作用。在这些蛋白质中,据报道,膜胆固醇结合并调节其运动的特定胆固醇结合基序。这种共有的基质被视为CRAC和CARC,其对应于一个和五个残基之间的任何氨基酸。因此,众所周知,重点是人类GPCR运输商,以确定GPCR家族的所有七个螺旋中这个主题的分配,并为单独的螺旋提供一个和谐签名主题。基于使用模糊C-Mircy的基于光谱聚类的计算方法已经尝试以获得来自GPCR超级家庭的胆固醇的异质类型。从获得的结果中,可以看出,在我们的数据集中排除嗅觉家族,我们发现胆固醇图案与GPCR系列的跨膜螺旋完美匹配,可以进一步扩展到其他膜蛋白。

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