PDBe工具对蛋白质数据库中的小分子进行深入分析。

IF 5.2 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Protein Science Pub Date : 2025-04-01 DOI:10.1002/pro.70084
Preeti Choudhary, Ibrahim Roshan Kunnakkattu, Sreenath Nair, Dare Kayode Lawal, Ivanna Pidruchna, Marcelo Querino Lima Afonso, Jennifer R Fleming, Sameer Velankar
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引用次数: 0

摘要

蛋白质数据库(PDB)是实验确定的生物大分子及其配体、蛋白质和核酸复合物的3D结构的主要全球存储库。PDB包含超过47000个与大分子结合的独特小分子。尽管有大量可用的数据,但PDB中小分子数据的复杂性需要专门的工具来进行有效的分析和可视化。PDBe已经开发了许多工具,包括用于访问和丰富配体数据的PDBe CCDUtils (https://github.com/PDBeurope/ccdutils),用于分析配体和大分子之间相互作用的PDBe Arpeggio (https://github.com/PDBeurope/arpeggio),以及用于识别配体(如反应物,辅因子或药物样分子)在蛋白质配体复合物中的功能作用的PDBe RelLig (https://github.com/PDBeurope/rellig)。这些工具生成的增强配体注释和数据呈现在新的pbe - kb配体页面上,提供了小分子的全面概述,并提供了对其生物学背景的有价值的见解(伊马替尼的示例页面:https://pdbe.org/chem/sti)。通过提高配体识别的标准化,添加各种注释,并提供先进的可视化功能,这些工具帮助研究人员导航小分子及其在生物系统中的作用的复杂性,促进对生物功能的机制理解。这些资源的持续增强旨在支持科学界获得对配体及其在各个领域的应用的有价值的见解,包括药物发现,分子生物学,系统生物学,结构生物学和药理学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PDBe tools for an in-depth analysis of small molecules in the Protein Data Bank.

The Protein Data Bank (PDB) is the primary global repository for experimentally determined 3D structures of biological macromolecules and their complexes with ligands, proteins, and nucleic acids. PDB contains over 47,000 unique small molecules bound to the macromolecules. Despite the extensive data available, the complexity of small-molecule data in the PDB necessitates specialized tools for effective analysis and visualization. PDBe has developed a number of tools, including PDBe CCDUtils (https://github.com/PDBeurope/ccdutils) for accessing and enriching ligand data, PDBe Arpeggio (https://github.com/PDBeurope/arpeggio) for analyzing interactions between ligands and macromolecules, and PDBe RelLig (https://github.com/PDBeurope/rellig) for identifying the functional roles of ligands (such as reactants, cofactors, or drug-like molecules) within protein-ligand complexes. The enhanced ligand annotations and data generated by these tools are presented on the novel PDBe-KB ligand pages, offering a comprehensive overview of small molecules and providing valuable insights into their biological contexts (example page for Imatinib: https://pdbe.org/chem/sti). By improving the standardization of ligand identification, adding various annotations, and offering advanced visualization capabilities, these tools help researchers navigate the complexities of small molecules and their roles in biological systems, facilitating mechanistic understanding of biological functions. The ongoing enhancements to these resources are designed to support the scientific community in gaining valuable insights into ligands and their applications across various fields, including drug discovery, molecular biology, systems biology, structural biology, and pharmacology.

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来源期刊
Protein Science
Protein Science 生物-生化与分子生物学
CiteScore
12.40
自引率
1.20%
发文量
246
审稿时长
1 months
期刊介绍: Protein Science, the flagship journal of The Protein Society, is a publication that focuses on advancing fundamental knowledge in the field of protein molecules. The journal welcomes original reports and review articles that contribute to our understanding of protein function, structure, folding, design, and evolution. Additionally, Protein Science encourages papers that explore the applications of protein science in various areas such as therapeutics, protein-based biomaterials, bionanotechnology, synthetic biology, and bioelectronics. The journal accepts manuscript submissions in any suitable format for review, with the requirement of converting the manuscript to journal-style format only upon acceptance for publication. Protein Science is indexed and abstracted in numerous databases, including the Agricultural & Environmental Science Database (ProQuest), Biological Science Database (ProQuest), CAS: Chemical Abstracts Service (ACS), Embase (Elsevier), Health & Medical Collection (ProQuest), Health Research Premium Collection (ProQuest), Materials Science & Engineering Database (ProQuest), MEDLINE/PubMed (NLM), Natural Science Collection (ProQuest), and SciTech Premium Collection (ProQuest).
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