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iGEMDOCK:一个利用药理学相互作用和筛选后分析增强 GEMDOCK 的图形化环境。

iGEMDOCK: a graphical environment of enhancing GEMDOCK using pharmacological interactions and post-screening analysis.

机构信息

Institute of Bioinformatics and Systems Biology, National Chiao Tung University, Hsinchu 30050, Taiwan.

出版信息

BMC Bioinformatics. 2011 Feb 15;12 Suppl 1(Suppl 1):S33. doi: 10.1186/1471-2105-12-S1-S33.

Abstract

BACKGROUND

Pharmacological interactions are useful for understanding ligand binding mechanisms of a therapeutic target. These interactions are often inferred from a set of active compounds that were acquired experimentally. Moreover, most docking programs loosely coupled the stages (binding-site and ligand preparations, virtual screening, and post-screening analysis) of structure-based virtual screening (VS). An integrated VS environment, which provides the friendly interface to seamlessly combine these VS stages and to identify the pharmacological interactions directly from screening compounds, is valuable for drug discovery.

RESULTS

We developed an easy-to-use graphic environment, iGEMDOCK, integrating VS stages (from preparations to post-screening analysis). For post-screening analysis, iGEMDOCK provides biological insights by deriving the pharmacological interactions from screening compounds without relying on the experimental data of active compounds. The pharmacological interactions represent conserved interacting residues, which often form binding pockets with specific physico-chemical properties, to play the essential functions of a target protein. Our experimental results show that the pharmacological interactions derived by iGEMDOCK are often hot spots involving in the biological functions. In addition, iGEMDOCK provides the visualizations of the protein-compound interaction profiles and the hierarchical clustering dendrogram of the compounds for post-screening analysis.

CONCLUSIONS

We have developed iGEMDOCK to facilitate steps from preparations of target proteins and ligand libraries toward post-screening analysis. iGEMDOCK is especially useful for post-screening analysis and inferring pharmacological interactions from screening compounds. We believe that iGEMDOCK is useful for understanding the ligand binding mechanisms and discovering lead compounds. iGEMDOCK is available at http://gemdock.life.nctu.edu.tw/dock/igemdock.php.

摘要

背景

药物相互作用对于理解治疗靶点的配体结合机制很有用。这些相互作用通常是从一组通过实验获得的活性化合物中推断出来的。此外,大多数对接程序松散地耦合了基于结构的虚拟筛选(VS)的各个阶段(结合部位和配体准备、虚拟筛选和筛选后分析)。一个集成的 VS 环境,为药物发现提供了有价值的价值,它提供了友好的界面,可以无缝地组合这些 VS 阶段,并直接从筛选化合物中识别药物相互作用。

结果

我们开发了一个易于使用的图形环境,iGEMDOCK,集成了 VS 阶段(从准备到筛选后分析)。对于筛选后分析,iGEMDOCK 通过从筛选化合物中推导药物相互作用,而不依赖于活性化合物的实验数据,提供了生物学见解。药物相互作用代表保守的相互作用残基,这些残基通常形成具有特定物理化学性质的结合口袋,发挥靶蛋白的基本功能。我们的实验结果表明,iGEMDOCK 推导的药物相互作用通常是涉及生物功能的热点。此外,iGEMDOCK 为筛选后分析提供了蛋白质-化合物相互作用图谱和化合物层次聚类树状图的可视化。

结论

我们开发了 iGEMDOCK,以促进从靶蛋白和配体文库的准备到筛选后分析的步骤。iGEMDOCK 特别适用于筛选后分析和从筛选化合物中推断药物相互作用。我们相信 iGEMDOCK 有助于理解配体结合机制和发现先导化合物。iGEMDOCK 可在 http://gemdock.life.nctu.edu.tw/dock/igemdock.php 上获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/50b4/3044289/83f63f86c2d7/1471-2105-12-S1-S33-1.jpg

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