PDB-BRE: A ligand-protein interaction binding residue extractor based on Protein Data Bank

Shutao Chen,Ke Yan,Bin Liu

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS(2024)

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摘要
Proteins typically exert their biological functions by interacting with other biomole-cules or ligands. The study of ligand-protein interactions is crucial in elucidating the biological mechanisms of proteins. Most existing studies have focused on analyzing ligand-protein interactions, and they ignore the additional situational of inserted and modified residues. Besides, the resources often support only a single ligand type and cannot obtain satisfied results in analyzing novel complexes. Therefore, it is impor-tant to develop a general analytical tool to extract the binding residues of ligand- protein interactions in complexes fully. In this study, we propose a ligand-protein interaction binding residue extractor (PDB-BRE), which can be used to automatically extract interacting ligand or protein-binding residues from complex three-dimensional (3D) structures based on the RCSB Protein Data Bank (RCSB PDB). PDB-BRE offers a notable advantage in its comprehensive support for analyzing six distinct types of ligands, including proteins, peptides, DNA, RNA, mixed DNA and RNA entities, and non-polymeric entities. Moreover, it takes into account the consid-eration of inserted and modified residues within complexes. Compared to other state-of-the-art methods, PDB-BRE is more suitable for massively parallel batch analy-sis, and can be directly applied for downstream tasks, such as predicting binding resi-dues of novel complexes. PDB-BRE is freely available at http://bliulab.net/PDB-BRE.
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关键词
binding residue extraction,ligand-protein interaction recognition,rule-based matching method,sequence label matching
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