The discovery of protein–ligand-binding sites is a major step for elucidating protein function and for investigating new functional roles. Detecting protein–ligand-binding sites experimentally is time-consuming and expensive. Thus, a variety of in silico methods to detect and predict binding sites was proposed as they can be scalable, fast and present low cost.

中文翻译：

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GRaSP：基于图的残基邻域策略，预测结合位点

蛋白质-配体结合位点的发现是阐明蛋白质功能和研究新功能的重要步骤。实验上检测蛋白质-配体结合位点既耗时又昂贵。因此，提出了多种用于检测和预测结合位点的计算机方法，因为它们可以扩展，快速并且具有低成本。