The proteasome-dependent proteolytic system

被引:38
作者
Tanahashi, N
Kawahara, H
Murakami, Y
Tanaka, K
机构
[1] Tokyo Metropolitan Inst Med Sci, Bunkyo Ku, Tokyo 1138613, Japan
[2] Japan Sci & Technol Corp, CREST, Bunkyo Ku, Tokyo 1138613, Japan
[3] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[4] Jikei Univ, Sch Med, Dept Biochem 2, Tokyo 1050003, Japan
关键词
D O I
10.1023/A:1006909522731
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
The 20S proteasome is an intriguingly large complex that acts as a proteolytic catalytic machine. Accumulating evidence indicates the existence of multiple factors capable of regulating the proteasome function. They are classified into two different categories, one type of regulator is PA700 or PA28 that is reversibly associated with the 20S proteasome to form enzymatically active proteasomes and the other type including a 300-kDa modulator and PI31 indirectly influences proteasome activity perhaps by promoting or suppressing the assembly of the 20S proteasome with PA700 or PA28. Thus, there have been documented two types of proteasomes composed of a core catalytic proteasome and a pair of symmetrically disposed PA700 or PA28 regulatory particle. Moreover, the recently-identified proteasome containing both PA28 and PA700 appears to play a significant role in the ATP-dependent proteolytic pathway in cells, as can the 26S proteasome which is known as a eukaryotic ATP-dependent protease.
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页码:3 / 9
页数:7
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