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IUPHAR-DB: An Expert-Curated, Peer-Reviewed Database of Receptors and Ion Channels

机译:IUPHAR-DB:一个经过专家评审,经过同行评审的受体和离子通道数据库

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摘要

The International Union of Basic and Clinical Pharmacology database (IUPHAR-DB) integrates peer-reviewed pharmacological, chemical, genetic, functional and anatomical information on the 354 non-sensory G protein-coupled receptors (GPCRs), 71 ligand-gated ion channel subunits and 141 voltage-gated ion channel subunits encoded by the human, rat and mouse genomes. These genes represent the targets of about a third of currently approved drugs and are a major focus of drug discovery and development programs in the pharmaceutical industry. Individual gene pages provide a comprehensive description of the genes and their functions, with information on protein structure, ligands, expression patterns, signaling mechanisms, functional assays and biologically important receptor variants (e.g. single nucleotide polymorphisms and splice variants). The phenotypes resulting from altered gene expression (e.g. in genetically altered animals) and genetic mutations are described. Links are provided to bioinformatics resources such as NCBI RefSeq, OMIM, PubChem, human, rat and mouse genome databases. Recent developments include the addition of ligand-centered pages summarising information about unique ligand molecules in IUPHAR-DB. IUPHAR-DB represents a novel approach to biocuration because most data are provided through manual curation of published literature by a network of over 60 expert subcommittees coordinated by NC-IUPHAR. Data are referenced to the primary literature and linked to PubMed. The data are checked to ensure accuracy and consistency by the curators, added to the production server using custom-built submission tools and peer-reviewed by NC-IUPHAR, before being transferred to the public database. Data are reviewed and updated regularly (at least biennially). Other website features include comprehensive database search tools, online and downloadable gene lists and links to recent publications of interest to the field, such as reports on receptor-ligand pairings. The database is freely available at "http://www.iuphar-db.org":http://www.iuphar-db.org. Curators can be reached at curators [at] iuphar-db.org. We thank British Pharmacological Society, UNESCO (through the ICSU Grants Programme), Incyte, GlaxoSmithKline, Novartis, Servier and Wyeth for their support.
机译:国际基础和临床药理学联合会数据库(IUPHAR-DB)整合了354种非感觉性G蛋白偶联受体(GPCR),71个配体门控离子通道亚基的同行评审药理,化学,遗传,功能和解剖学信息以及由人类,大鼠和小鼠基因组编码的141个电压门控离子通道亚基。这些基因代表了目前批准的约三分之一药物的靶标,并且是制药行业药物发现和开发计划的主要重点。各个基因页面提供了有关基因及其功能的全面描述,并提供了有关蛋白质结构,配体,表达模式,信号转导机制,功能测定和生物学上重要的受体变体(例如单核苷酸多态性和剪接变体)的信息。描述了由基因表达改变(例如在遗传改变的动物中)和遗传突变产生的表型。提供到生物信息学资源的链接,例如NCBI RefSeq,OMIM,PubChem,人类,大鼠和小鼠基因组数据库。最近的发展包括添加了以配体为中心的页面,这些页面总结了有关IUPHAR-DB中独特配体分子的信息。 IUPHAR-DB代表了一种新的生物固化方法,因为大多数数据是通过由NC-IUPHAR协调的60多个专家小组委员会的网络通过人工整理出版的文献来提供的。数据参考了主要文献并链接到PubMed。策展人检查数据以确保准确性和一致性,然后使用定制构建的提交工具将数据添加到生产服务器中,并由NC-IUPHAR进行同行评审,然后再传输到公共数据库。定期(至少每两年一次)检查和更新数据。其他网站功能还包括全面的数据库搜索工具,在线和可下载的基因列表,以及该领域最近关注的出版物的链接,例如有关受体-配体配对的报告。该数据库可从“ http://www.iuphar-db.org”免费获得:http://www.iuphar-db.org。可以通过iuphar-db.org的策展人与策展人联系。我们感谢英国药理学会,教科文组织(通过ICSU赠款计划),Incyte,葛兰素史克,诺华,Servier和惠氏提供的支持。

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