G. SusanaMedina, A. V. Fassio, S. Silveira, C. H. Silveira, R. Minardi
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引用次数: 2
摘要
蛋白质-配体相互作用(PLI)网络显示了蛋白质如何通过非共价键与小的非蛋白质配体相互作用。了解这种相互作用是迈向配体预测、靶标识别和药物设计的关键一步。我们提出了CALI (Complex network-based Analysis of protein-Ligand Interactions),这是一种基于图的视觉策略,结合复杂的网络拓扑特性来总结和检测pli中的频繁模式。将CALI获得的模式与CDK2和蓖麻毒素数据集中实验确定的蛋白质-配体相互作用进行比较。对于CDK2, CALI发现了90%的相互作用残基,以及所有与配体相互作用的蓖麻毒素残基。我们设计了一个强大的可视化和交互式策略来分析数据,提供交互数据集的一般视图,从全球角度显示最常见的pli。
CALI: A Novel Visual Model for Frequent Pattern Mining in Protein-Ligand Graphs
Protein-ligand interaction (PLI) networks show how proteins interact with small non-protein ligands through noncovalent bonding. Understanding such interactions is a crucial step towards ligand prediction, target identification and drug design. We propose CALI (Complex network-based Analysis of protein-Ligand Interactions), a graph-based, visual strategy coupled with complex network topological properties to summarize and detect frequent patterns in PLIs. Patterns obtained with CALI were compared to experimentally determined protein-ligand interactions from the CDK2 and Ricin dataset. For the CDK2, CALI found 90% of interacting residues, and all residues of the Ricin that interact with ligands. We devised a powerful visual and interactive strategy to analyze the data, providing a general view of the interaction dataset, showing the most common PLIs from a global perspective.