PREDDIMER: a web server for prediction of transmembrane helical dimers

被引:71
作者
Polyansky, Anton A. [1 ,2 ]
Chugunov, Anton O. [1 ]
Volynsky, Pavel E. [1 ]
Krylov, Nikolay A. [1 ]
Nolde, Dmitry E. [1 ]
Efremov, Roman G. [1 ,3 ]
机构
[1] Russian Acad Sci, MM Shemyakin & Yu A Ovchinnikov Inst Bioorgan Che, Moscow 117997, Russia
[2] Univ Vienna, Dept Struct & Computat Biol, Max F Perutz Labs, AT-1030 Vienna, Austria
[3] State Univ, Moscow Inst Phys & Technol, Dolgoprudnyi 141700, Moscow Region, Russia
基金
俄罗斯基础研究基金会;
关键词
ACTIVATION; DIMERIZATION; MEMBRANE; RECEPTOR; DOMAINS;
D O I
10.1093/bioinformatics/btt645
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Here we present PREDDIMER, a web tool for prediction of dimer structure of transmembrane (TM) helices. PREDDIMER allows (i) reconstruction of a number of dimer structures for given sequence(s) of TM protein fragments, (ii) ranking and filtering of predicted structures according to respective values of a scoring function, (iii) visualization of predicted 3D dimer structures and (iv) visualization of surface hydrophobicity of TM helices and their contacting (interface) regions represented as 2D maps. Results: We implemented online the original PREDDIMER algorithm and benchmarked the server on 11 TM sequences, whose 3D dimer conformations were obtained previously by nuclear magnetic resonance spectroscopy. In the most of tested cases backbone root-mean-square deviations of closest predicted conformations from the experimental reference are below 3 A. A randomization test displays good anticorrelation (-0.82) between values of the scoring function and statistical significance of the prediction 'by chance'. Going beyond a single dimer conformation, our web tool predicts an ensemble of possible conformations, which may be useful for explanation of a functioning of bitopic membrane proteins, e.g. receptor tyrosine kinases.
引用
收藏
页码:889 / 890
页数:2
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