PDEStrIAn: A Phosphodiesterase Structure and Ligand Interaction Annotated Database As a Tool for Structure-Based Drug Design

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• 作者：Chimed Jansen ; Albert J. Kooistra ; Georgi K. Kanev ; Rob Leurs ; Iwan J. P. de Esch ; Chris de Graaf
• 刊名：Journal of Medicinal Chemistry
• 出版年：2016
• 出版时间：August 11, 2016
• 年：2016
• 卷：59
• 期：15
• 页码：7029-7065
• 全文大小：4713K
• 年卷期：0
• ISSN：1520-4804

文摘

A systematic analysis is presented of the 220 phosphodiesterase (PDE) catalytic domain crystal structures present in the Protein Data Bank (PDB) with a focus on PDE–ligand interactions. The consistent structural alignment of 57 PDE ligand binding site residues enables the systematic analysis of PDE–ligand interaction fingerprints (IFPs), the identification of subtype-specific PDE–ligand interaction features, and the classification of ligands according to their binding modes. We illustrate how systematic mining of this phosphodiesterase structure and ligand interaction annotated (PDEStrIAn) database provides new insights into how conserved and selective PDE interaction hot spots can accommodate the large diversity of chemical scaffolds in PDE ligands. A substructure analysis of the cocrystallized PDE ligands in combination with those in the ChEMBL database provides a toolbox for scaffold hopping and ligand design. These analyses lead to an improved understanding of the structural requirements of PDE binding that will be useful in future drug discovery studies.