MECHANISM OF SPECIFIC LEXA CLEAVAGE - AUTODIGESTION AND THE ROLE OF RECA COPROTEASE

被引:286
作者
LITTLE, JW [1 ]
机构
[1] UNIV ARIZONA, DEPT MOLEC & CELLULAR BIOL, TUCSON, AZ 85721 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SOS REGULATORY SYSTEM; SELF-PROCESSING; INTRAMOLECULAR REACTION; SERINE PROTEASE; IND(S) MUTATIONS;
D O I
10.1016/0300-9084(91)90108-D
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
Specific LexA cleavage can occur under two different conditions: RecA-mediated cleavage requires an activated form of RecA, while an intramolecular self-cleavage termed autodigestion proceeds spontaneously at high pH and does not involve RecA. The two cleavage reactions are closely related. We postulate that RecA stimulates autodigestion rather than acting as a typical protease, and it is proposed to term this activity 'RecA coprotease' to emphasize this indirect role. The mechanism of autodigestion is similar to that of a serine protease, and RecA appears to act by reducing the pK(a) of a critical lysine residue LexA. A new class of mutants, termed lexA (Ind(S)), is described; these mutations increase the rate of LexA cleavage.
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页码:411 / 422
页数:12
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