The computational prediction of protein assemblies

被引:3
|
作者
Tramontanol, Anna [1 ,2 ]
机构
[1] Sapienza Univ Rome, Phys Dept, Piazzale Aldo Moro 5, I-00185 Rome, Italy
[2] Sapienza Univ Rome, Fdn Cenci Bolognetti, Ist Pasteur, Piazzale Aldo Moro 5, I-00185 Rome, Italy
关键词
CORRELATED MUTATIONS; INTERACTION DATABASE; DOCKING; CAPRI; COMPLEXES; CONTACTS; INTERACTOME; ALGORITHMS; PROGRESS; GENOMES;
D O I
10.1016/j.sbi.2017.10.006
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
The function of proteins in the cell is almost always mediated by their interaction with different partners, including other proteins, nucleic acids or small organic molecules. The ability of identifying all of them is an essential step in our quest for understanding life at the molecular level. The inference of the protein complex composition and of its molecular details can also provide relevant clues for the development and the design of drugs. In this short review, I will discuss the computational aspects of the analysis and prediction of protein-protein assemblies and discuss some of the most recent developments as seen in the last Critical Assessment of Techniques for Protein Structure Prediction (GASP) experiment.
引用
收藏
页码:170 / 175
页数:6
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