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

被引:2
作者
Chen, Shutao [1 ]
Yan, Ke [1 ,3 ]
Liu, Bin [1 ,2 ,3 ]
机构
[1] Beijing Inst Technol, Sch Comp Sci & Technol, Beijing, Peoples R China
[2] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, Beijing, Peoples R China
[3] Beijing Inst Technol, Zhongguancun South St, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
binding residue extraction; ligand-protein interaction recognition; rule-based matching method; sequence label matching; CHEMISTRY; GENE;
D O I
10.1002/prot.26596
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:145 / 153
页数:9
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