CyBase: a database of cyclic protein sequences and structures, with applications in protein discovery and engineering

被引:232
|
作者
Wang, Conan K. L. [1 ]
Kaas, Quentin [1 ]
Chiche, Laurent [2 ]
Craik, David J. [1 ]
机构
[1] Univ Queensland, Ctr Funct & Appl Genom, Australia Res Council Special Res, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Montpellier, CNRS, UMR 5048, Ctr Biochim Struct,INSERM3,U554, F-34090 Montpellier, France
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
D O I
10.1093/nar/gkm953
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
CyBase was originally developed as a database for backbone-cyclized proteins, providing search and display capabilities for sequence, structure and function data. Cyclic proteins are interesting because, compared to conventional proteins, they have increased stability and enhanced binding affinity and therefore can potentially be developed as protein drugs. The new CyBase release features a redesigned interface and internal architecture to improve user-interactivity, collates double the amount of data compared to the initial release, and hosts a novel suite of tools that are useful for the visualization, characterization and engineering of cyclic proteins. These tools comprise sequence/structure 2D representations, a summary of grafting and mutation studies of synthetic analogues, a study of N- to C-terminal distances in known protein structures and a structural modelling tool to predict the best linker length to cyclize a protein. These updates are useful because they have the potential to help accelerate the discovery of naturally occurring cyclic proteins and the engineering of cyclic protein drugs. The new release of CyBase is available at http://research1t.imb.uq.edu.au/cybase.
引用
收藏
页码:D206 / D210
页数:5
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