首页> 外文会议>EvoWorkshops 2006: EvoBIO, EvoCOMNET, EvoHOT, EvoIASP, EvoINTERACTION, EvoMUSART, and EvoSTOC; 20060410-12; Budapest(HU) >Functional Classification of G-Protein Coupled Receptors, Based on Their Specific Ligand Coupling Patterns
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Functional Classification of G-Protein Coupled Receptors, Based on Their Specific Ligand Coupling Patterns

机译:G-蛋白偶联受体的功能分类,基于其特定的配体偶联模式

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摘要

Functional identification of G-Protein Coupled Receptors (GPCRs) is one of the current focus areas of pharmaceutical research. Although thousands of GPCR sequences are known, many of them remain as orphan sequences (the activating ligand is unknown). Therefore, classification methods for automated characterization of orphan GPCRs are imperative. In this study, for predicting Level 2 subfamilies of Amine GPCRs, a novel method for obtaining fixed-length feature vectors, based on the existence of activating ligand specific patterns, has been developed and utilized for a Support Vector Machine (SVM)-based classification. Exploiting the fact that there is a non-promiscuous relationship between the specific binding of GPCRs into their ligands and their functional classification, our method classifies Level 2 subfamilies of Amine GPCRs with a high predictive accuracy of 97.02% in a ten-fold cross validation test. The presented machine learning approach, bridges the gulf between the excess amount of GPCR sequence data and their poor functional characterization.
机译:G蛋白偶联受体(GPCR)的功能鉴定是药物研究的当前重点领域之一。尽管成千上万的GPCR序列是已知的,但其中许多仍保留为孤立序列(激活配体是未知的)。因此,用于自动表征孤儿GPCR的分类方法势在必行。在这项研究中,为预测胺GPCR的2级亚家族,基于活化配体特异性模式的存在,开发了一种获取固定长度特征向量的新方法,并将其用于基于支持向量机(SVM)的分类。利用GPCR与配体的特异性结合与其功能分类之间不存在混杂关系这一事实,我们的方法在十倍交叉验证测试中对胺GPCR的2级亚家族进行了分类,预测准确性高达97.02% 。提出的机器学习方法在过量的GPCR序列数据与不良的功能表征之间架起了桥梁。

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