EDM-DEDM and protein crystal structure solution

被引:13
作者
Caliandro, Rocco [1 ]
Carrozzini, Benedetta [1 ]
Cascarano, Giovanni Luca [1 ]
Giacovazzo, Carmelo [1 ]
Mazzone, Anna Maria [1 ]
Siliqi, Dritan [1 ]
机构
[1] CNR, Inst Crystallog, I-70126 Bari, Italy
来源
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY | 2009年 / 65卷
关键词
X-RAY-DIFFRACTION; MOLECULAR-REPLACEMENT; STRUCTURE PREDICTION; DENSITY MODIFICATION; STRUCTURE REFINEMENT; RESOLUTION; SOFTWARE; SEARCH; COMBINATION; EXTENSION;
D O I
10.1107/S0907444909008609
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Electron-density modification (EDM) procedures are the classical tool for driving model phases closer to those of the target structure. They are often combined with automated model-building programs to provide a correct protein model. The task is not always performed, mostly because of the large initial phase error. A recently proposed procedure combined EDM with DEDM (difference electron-density modification); the method was applied to the refinement of phases obtained by molecular replacement, ab initio or SAD phasing [Caliandro, Carrozzini, Cascarano, Giacovazzo, Mazzone & Siliqi (2009), Acta Cryst. D65, 249-256] and was more effective in improving phases than EDM alone. In this paper, a novel fully automated protocol for protein structure refinement based on the iterative application of automated model-building programs combined with the additional power derived from the EDM-DEDM algorithm is presented. The cyclic procedure was successfully tested on challenging cases for which all other approaches had failed.
引用
收藏
页码:477 / 484
页数:8
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