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Determinig the ligand-specific regions of peptide-binding G-Protein Coupled Receptors

机译:确定肽结合G蛋白偶联受体的配体特异性区域

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The G-Protein Coupled Receptor (GPCR) proteins are of paramount importance for pharmaceutical research as this single family of proteins is targeted by more than 50% of all modern drugs. Their ligands include but are not limited to small molecules, peptides and photons. Consequently it is vital to know the sites of interaction between the ligand and the receptor. These sites can be used for a multitude of purposes such as classification of sequences or drug design. We use the feature extraction method proposed in [1] to analyze the ligand-specific regions among various Peptide-binding GPCRs. We present the features that will help drug design researchers enhance specificity of peptide-binding drugs.
机译:G蛋白偶联受体(GPCR)蛋白在药物研究中至关重要,因为该单一蛋白家族被所有现代药物中超过50%靶向。它们的配体包括但不限于小分子,肽和光子。因此,了解配体与受体之间的相互作用位点至关重要。这些位点可用于多种目的,例如序列分类或药物设计。我们使用[1]中提出的特征提取方法来分析各种肽结合GPCR之间的配体特异性区域。我们提出的功能将帮助药物设计研究人员增强肽结合药物的特异性。

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