GPCRdb: an information system for G protein-coupled receptors

被引:228
作者
Isberg, Vignir [1 ]
Mordalski, Stefan [2 ]
Munk, Christian [1 ]
Rataj, Krzysztof [2 ]
Harpsoe, Kasper [1 ]
Hauser, Alexander S. [1 ]
Vroling, Bas [3 ]
Bojarski, Andrzej J. [2 ]
Vriend, Gert [4 ]
Gloriam, David E. [1 ]
机构
[1] Univ Copenhagen, Dept Drug Design & Pharmacol, Jagtvej 162, DK-2100 Copenhagen, Denmark
[2] Polish Acad Sci, Inst Pharmacol, Dept Med Chem, Smetna 12, PL-31343 Krakow, Poland
[3] Bioprodict BV, Nieuwe Markstr 54E, NL-6511 AA Nijmegen, Netherlands
[4] Radboud Univ Nijmegen, CMBI, NCMLS, Med Ctr, Geert Grootepl Zuid 26-28, NL-6525 GA Nijmegen, Netherlands
基金
欧洲研究理事会;
关键词
CRYSTAL-STRUCTURE; ALLOSTERIC MODULATION; OPIOID RECEPTOR; DATABASE; FAMILY; ACTIVATION; LIGANDS; DOCKING;
D O I
10.1093/nar/gkv1178
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
Recent developments in G protein-coupled receptor (GPCR) structural biology and pharmacology have greatly enhanced our knowledge of receptor structure-function relations, and have helped improve the scientific foundation for drug design studies. The GPCR database, GPCRdb, serves a dual role in disseminating and enabling new scientific developments by providing reference data, analysis tools and interactive diagrams. This paper highlights new features in the fifth major GPCRdb release: (i) GPCR crystal structure browsing, superposition and display of ligand interactions; (ii) direct deposition by users of point mutations and their effects on ligand binding; (iii) refined snake and helix box residue diagram looks; and (iii) phylogenetic trees with receptor classification colour schemes. Under the hood, the entire GPCRdb front-and back-ends have been recoded within one infrastructure, ensuring a smooth browsing experience and development. GPCRdb is available at http://www.gpcrdb.org/ and it's open source code at https://bitbucket.org/gpcr/protwis.
引用
收藏
页码:D356 / D364
页数:9
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