Intramembrane Proteolysis by Signal Peptide Peptidases: A Comparative Discussion of GXGD-type Aspartyl Proteases

被引:54
作者
Fluhrer, Regina [1 ]
Steiner, Harald
Haass, Christian
机构
[1] Univ Munich, DZNE, D-80336 Munich, Germany
关键词
GAMMA-SECRETASE ACTIVITY; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; PRESENILIN HOMOLOGS; CAENORHABDITIS-ELEGANS; TNF-ALPHA; CLEAVAGE; NICASTRIN; INHIBITOR; PROTEIN; SPPL2B;
D O I
10.1074/jbc.R800040200
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
Intramembrane-cleaving proteases are required for reverse signaling and membrane protein degradation. A major class of these proteases is represented by the GXGD-type aspartyl proteases. GXGD describes a novel signature sequence that distinguishes these proteases from conventional aspartyl proteases. Members of the family of the GXGD-type aspartyl proteases are the Alzheimer disease-related gamma-secretase, the signal peptide peptidases and their homologs, and the bacterial type IV prepilin peptidases. We will describe the major biochemical and functional properties of the signal peptide peptidases and their relatives. We then compare these properties with those of gamma-secretase and discuss common mechanisms but also point out a number of substantial differences.
引用
收藏
页码:13975 / 13979
页数:5
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