Computational approaches to macromolecular interactions in the cell

被引:11
|
作者
Vakser, Ilya A. [1 ]
Deeds, Eric J. [1 ]
机构
[1] Univ Kansas, Computat Biol Program, Lawrence, KS 66045 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
STRUCTURE PREDICTION; BACTERIAL CYTOPLASM; PROTEIN DOCKING; RNA; COMPLEXES; BINDING; MODELS; ENVIRONMENTS; SIMULATION; SEQUENCE;
D O I
10.1016/j.sbi.2019.03.012
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
Structural modeling of a cell is an evolving strategic direction in computational structural biology. It takes advantage of new powerful modeling techniques, deeper understanding of fundamental principles of molecular structure and assembly, and rapid growth of the amount of structural data generated by experimental techniques. Key modeling approaches to principal types of macromolecular assemblies in a cell already exist. The main challenge, along with the further development of these modeling approaches, is putting them together in a consistent, unified whole cell model. This opinion piece addresses the fundamental aspects of modeling macromolecular assemblies in a cell, and the state-of-the-art in modeling of the principal types of such assemblies.
引用
收藏
页码:59 / 65
页数:7
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