Fast estimation of surface complementarity in protein complexes

被引:0
|
作者
Franzot, G
Carugo, O
机构
[1] Scuola Int Super Studi Avanzati, I-34014 Trieste, Italy
[2] Sincrotrone Trieste, I-34012 Trieste, Italy
[3] Univ Pavia, Dept Gen Chem, I-27100 Pavia, Italy
[4] TASC INFM Natl Lab, I-34012 Trieste, Italy
关键词
protein structure; protein-protein interaction; protein surface;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel measure of protein surface complementarity, sc_pride, is proposed. Each surface patch is represented by the distribution of the inter-atomic distances and the degree of similarity between two surface patches is estimated via a contingency table analysis of their two inter-atomic distance distributions. Such a low resolution surface representation allows very fast complementarity estimations that could find applications in protein-protein interaction prediction. The performance of sc_pride is compared to that of other surface complementarity measures with a very large set of protein-protein complexes obtained with docking simulations and the ability of sc_pride to recognize the surface complementarity is tested on a non-redundant set of experimentally determined crystal structures of protein-protein complexes.
引用
收藏
页码:231 / 243
页数:13
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