Protein-Protein Interactions and Multi-component Complexes of Aminoacyl-tRNA Synthetases

被引:31
作者
Kim, Jong Hyun [1 ]
Han, Jung Min [2 ]
Kim, Sunghoon [1 ]
机构
[1] Seoul Natl Univ, Coll Pharm, Grad Sch Convergence Sci & Technol, Med Bioconvergence Res Ctr, Seoul 151742, South Korea
[2] Yonsei Univ, Coll Pharm, Dept Integrated OMICS Biomed Sci, Seoul 120749, South Korea
来源
AMINOACYL-TRNA SYNTHETASES IN BIOLOGY AND MEDICINE | 2014年 / 344卷
关键词
Aminoacyl-tRNA synthetase; Multi-tRNA synthetase complex; Protein-protein interaction; MACROMOLECULAR ASSEMBLAGE; NONCANONICAL FUNCTION; UBIQUITIN LIGASE; FAMILY PROTEINS; DOWN-REGULATION; VE-CADHERIN; P53; TRANSLATION; RECEPTOR; GP96;
D O I
10.1007/128_2013_479
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Protein-protein interaction occurs transiently or stably when two or more proteins bind together to mediate a wide range of cellular processes such as protein modification, signal transduction, protein trafficking, and structural folding. The macromolecules involved in protein biosynthesis such as aminoacyl-tRNA synthetase (ARS) have a number of protein-protein interactions. The mammalian multi-tRNA synthetase complex (MSC) consists of eight different enzymes: EPRS, IRS, LRS, QRS, MRS, KRS, RRS, and DRS, and three auxiliary proteins: AIMP1/p43, AIMP2/p38, and AIMP/p18. The distinct ARS proteins are also connected to diverse protein networks to carry out biological functions. In this chapter we first show the protein networks of the entire MSC and explain how MSC components interact with or can regulate other proteins. Finally, it is pointed out that the understanding of protein-protein interaction mechanism will provide insight to potential therapeutic application for diseases related to the MSC network.
引用
收藏
页码:119 / 144
页数:26
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