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氨酰-tRNA 合成酶:结构、功能与药物发现。

Aminoacyl-tRNA synthetases: Structure, function, and drug discovery.

机构信息

Molecular and Structural Biophysics Laboratory, Department of Biochemistry, North-Eastern Hill University, Shillong, Meghalaya, India.

Department of Biotechnology, National Institute of Technology, Raipur, India.

出版信息

Int J Biol Macromol. 2018 May;111:400-414. doi: 10.1016/j.ijbiomac.2017.12.157. Epub 2018 Jan 3.

Abstract

Aminoacyl-tRNA synthetases (AARSs) are the enzymes that catalyze the aminoacylation reaction by covalently linking an amino acid to its cognate tRNA in the first step of protein translation. Beyond this classical function, these enzymes are also known to have a role in several metabolic and signaling pathways that are important for cell viability. Study of these enzymes is of great interest to the researchers due to its pivotal role in the growth and survival of an organism. Further, unfolding the interesting structural and functional aspects of these enzymes in the last few years has qualified them as a potential drug target against various diseases. Here we review the classification, function, and the conserved as well the appended structural architecture of these enzymes in detail, including its association with multi-synthetase complexes. We also considered their role in human diseases in terms of mutations and autoantibodies against AARSs. Finally, we have discussed the available inhibitors against AARSs. This review offers comprehensive information on AARSs under a single canopy that would be a good inventory for researchers working in this area.

摘要

氨酰-tRNA 合成酶(AARSs)是在蛋白质翻译的第一步中通过共价连接氨基酸与其相应的 tRNA 将其氨酰化的酶。除了这种经典功能外,这些酶还已知在几种代谢和信号通路中发挥作用,这些通路对细胞活力很重要。由于这些酶在生物体的生长和存活中起着关键作用,因此研究这些酶引起了研究人员的极大兴趣。此外,在过去几年中揭示了这些酶有趣的结构和功能方面,使它们成为针对各种疾病的潜在药物靶标。在这里,我们详细回顾了这些酶的分类、功能以及保守和附加的结构架构,包括它们与多合成酶复合物的关联。我们还根据突变和针对 AARSs 的自身抗体讨论了它们在人类疾病中的作用。最后,我们讨论了针对 AARSs 的可用抑制剂。该综述在一个单一的保护伞下提供了有关 AARSs 的全面信息,这将是该领域研究人员的良好库存。

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