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An Augmented Pocketome: Detection and Analysis of Small-Molecule Binding Pockets in Proteins of Known 3D Structure

机译:一种增强的女性小编:已知3D结构蛋白质中小分子绑定口袋的检测和分析

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摘要

Protein-ligand interactions form the basis of most cellular events. Identifying ligand binding pockets in proteins will greatly facilitate rationalizing and predicting protein function. Ligand binding sites are unknown for many proteins of known three-dimensional (3D) structure, creating a gap in our understanding of protein structure-function relationships. To bridge this gap, we detect pockets in proteins of known 3D structures, using computational techniques. This augmented pocketome (PocketDB) consists of 249,096 pockets, which is about seven times larger than what is currently known. We deduce possible ligand associations for about 46% of the newly identified pockets. The augmented pocketome, when subjected to clustering based on similarities among pockets, yielded 2,161 site types, which are associated with 1,037 ligand types, together providing fold-site-type-ligand-type associations. The PocketDB resource facilitates a structure-based function annotation, delineation of the structural basis of ligand recognition, and provides functional clues for domains of unknown functions, allosteric proteins, and druggable pockets.
机译:蛋白质 - 配体相互作用形成大多数细胞事件的基础。鉴定蛋白质中的配体结合袋将极大地促进合理化和预测蛋白质功能。对于已知的三维(3D)结构的许多蛋白质,配体结合位点是未知的,在我们对蛋白质结构功能关系的理解中产生间隙。为了弥合这种差距,我们使用计算技术检测已知3D结构的蛋白质中的口袋。这款增强的女性面包(PocketDB)由249,096个口袋组成,比目前已知的大约七倍。我们推导出可能的配体关联约46%的新已识别的口袋。当基于口袋之间的相似性进行聚类时,增强的Pocketome产生了2,161种,其与1,037个配体类型相关联,一起提供折叠部位类型 - 配体型关联。 PocketDB资源有助于基于结构的函数注释,描绘配体识别的结构基础,并为未知功能,变构蛋白和可药袋的结构域提供功能线索。

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