Protein Splicing: How Inteins Escape from Precursor Proteins

被引:109
作者
Mills, Kenneth V. [1 ]
Johnson, Margaret A. [2 ]
Perler, Francine B. [3 ]
机构
[1] Coll Holy Cross, Dept Chem, Worcester, MA 01610 USA
[2] Univ Alabama Birmingham, Dept Chem, Birmingham, AL 35294 USA
[3] New England Biolabs Inc, Ipswich, MA 01938 USA
基金
美国国家科学基金会;
关键词
TUBERCULOSIS-RECA INTEIN; BRANCHED INTERMEDIATE FORMATION; SYNECHOCYSTIS SP PCC6803; YEAST VMA1 PROTOZYME; C-TERMINAL CLEAVAGE; SSP DNAE INTEIN; MYCOBACTERIUM-TUBERCULOSIS; SACCHAROMYCES-CEREVISIAE; CRYSTAL-STRUCTURE; VMA1-DERIVED ENDONUCLEASE;
D O I
10.1074/jbc.R113.540310
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
Inteins are nature's escape artists; they facilitate their excision from flanking polypeptides (exteins) concomitant with extein ligation to produce a mature host protein. Splicing requires sequential nucleophilic displacement reactions catalyzed by strategies similar to proteases and asparagine lyases. Inteins require precise reaction coordination rather than rapid turnover or tight substrate binding because they are single turnover enzymes with covalently linked substrates. This has allowed inteins to explore alternative mechanisms with different steps or to use different methods for activation and coordination of the steps. Pressing issues include understanding the underlying details of catalysis and how the splicing steps are controlled.
引用
收藏
页码:14498 / 14505
页数:8
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