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核酶的结构、折叠与作用机制

Structure, folding and mechanisms of ribozymes.

作者信息

Lilley David M J

机构信息

Cancer Research UK Nucleic Acid Structure Research Group, University of Dundee, Dundee DD1 5EH, UK.

出版信息

Curr Opin Struct Biol. 2005 Jun;15(3):313-23. doi: 10.1016/j.sbi.2005.05.002.

Abstract

The past two years have seen exciting developments in RNA catalysis. A completely new ribozyme (possibly two) has come along and several new structures have been determined, including three different group I intron species. Although the origins of catalysis remain incompletely understood, a significant convergence of views has happened in the past year, together with the discovery of new super-fast ribozymes. There is persuasive evidence of general acid-base chemistry in nucleolytic ribozymes, whereas catalysis of peptidyl transfer in the ribosome seems to result largely from orientation and proximity effects. Lastly, important new folding-enhancing elements have been discovered.

摘要

在过去两年里,RNA催化领域取得了令人振奋的进展。出现了一种全新的核酶(可能是两种),并且确定了几种新结构,包括三种不同类型的I组内含子。尽管催化作用的起源仍未完全明晰,但在过去一年里,观点已显著趋同,同时还发现了新型超快速核酶。有确凿证据表明,核酸裂解核酶中存在一般酸碱化学作用,而核糖体中肽基转移的催化作用似乎主要源于定向和邻近效应。最后,还发现了重要的新型折叠增强元件。

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