Suppr超能文献

RCSB 蛋白质数据库:推动生物医学研究和药物发现。

RCSB Protein Data Bank: Enabling biomedical research and drug discovery.

机构信息

Research Collaboratory for Structural Bioinformatics Protein Data Bank, Rutgers, The State University of New Jersey, Piscataway, New Jersey.

Institute for Quantitative Biomedicine, Rutgers, The State University of New Jersey, Piscataway, New Jersey.

出版信息

Protein Sci. 2020 Jan;29(1):52-65. doi: 10.1002/pro.3730. Epub 2019 Nov 29.

Abstract

Analyses of publicly available structural data reveal interesting insights into the impact of the three-dimensional (3D) structures of protein targets important for discovery of new drugs (e.g., G-protein-coupled receptors, voltage-gated ion channels, ligand-gated ion channels, transporters, and E3 ubiquitin ligases). The Protein Data Bank (PDB) archive currently holds > 155,000 atomic-level 3D structures of biomolecules experimentally determined using crystallography, nuclear magnetic resonance spectroscopy, and electron microscopy. The PDB was established in 1971 as the first open-access, digital-data resource in biology, and is now managed by the Worldwide PDB partnership (wwPDB; wwPDB.org). US PDB operations are the responsibility of the Research Collaboratory for Structural Bioinformatics PDB (RCSB PDB). The RCSB PDB serves millions of RCSB.org users worldwide by delivering PDB data integrated with ∼40 external biodata resources, providing rich structural views of fundamental biology, biomedicine, and energy sciences. Recently published work showed that the PDB archival holdings facilitated discovery of ∼90% of the 210 new drugs approved by the US Food and Drug Administration 2010-2016. We review user-driven development of RCSB PDB services, examine growth of the PDB archive in terms of size and complexity, and present examples and opportunities for structure-guided drug discovery for challenging targets (e.g., integral membrane proteins).

摘要

对公开可用的结构数据的分析揭示了一些有趣的见解,这些见解涉及到对新药物发现具有重要意义的三维(3D)蛋白质靶标结构的影响(例如,G 蛋白偶联受体、电压门控离子通道、配体门控离子通道、转运蛋白和 E3 泛素连接酶)。蛋白质数据库(PDB)档案目前包含超过 155,000 个使用晶体学、核磁共振波谱学和电子显微镜术实验确定的生物分子的原子级 3D 结构。PDB 于 1971 年成立,是生物学领域的第一个开放获取、数字数据资源,现在由全球 PDB 合作伙伴(wwPDB;wwPDB.org)管理。美国 PDB 的运作由结构生物信息学研究合作组织 PDB(RCSB PDB)负责。RCSB PDB 通过提供与约 40 个外部生物数据资源集成的 PDB 数据,为基础生物学、生物医学和能源科学提供丰富的结构视图,为数百万的 RCSB.org 用户提供服务。最近的研究工作表明,PDB 档案的保存有助于发现 2010 年至 2016 年期间美国食品和药物管理局批准的 210 种新药中的约 90%。我们回顾了 RCSB PDB 服务的用户驱动型开发,考察了 PDB 档案在规模和复杂性方面的增长,并介绍了针对具有挑战性的靶标(例如,整合膜蛋白)的基于结构的药物发现的实例和机会。

相似文献

引用本文的文献

本文引用的文献

1
2
Molecular mechanisms of cereblon-based drugs.基于 cereblon 的药物的分子机制。
Pharmacol Ther. 2019 Oct;202:132-139. doi: 10.1016/j.pharmthera.2019.06.004. Epub 2019 Jun 14.
3
An outlook on using serial femtosecond crystallography in drug discovery.展望药物研发中连续的飞秒晶体学的应用。
Expert Opin Drug Discov. 2019 Sep;14(9):933-945. doi: 10.1080/17460441.2019.1626822. Epub 2019 Jun 11.
4
Voltage-gated sodium channels: structures, functions, and molecular modeling.电压门控钠离子通道:结构、功能与分子建模。
Drug Discov Today. 2019 Jul;24(7):1389-1397. doi: 10.1016/j.drudis.2019.05.014. Epub 2019 May 23.
5
Nav1.7 withholds its pain potential.Nav1.7抑制其引发疼痛的可能性。
Nat Rev Drug Discov. 2019 Apr 8. doi: 10.1038/d41573-019-00065-0.
6
7
Adhesion G Protein-Coupled Receptors as Drug Targets for Neurological Diseases.黏附 G 蛋白偶联受体作为神经疾病的药物靶点。
Trends Pharmacol Sci. 2019 Apr;40(4):278-293. doi: 10.1016/j.tips.2019.02.003. Epub 2019 Mar 11.
8
Structure and mechanism of AMPA receptor - auxiliary protein complexes.AMPA 受体 - 辅助蛋白复合物的结构与机制。
Curr Opin Struct Biol. 2019 Feb;54:104-111. doi: 10.1016/j.sbi.2019.01.011. Epub 2019 Feb 27.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验