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Endoplasmic reticulum aminopeptidases: biochemistry, physiology and pathology.

Authors :
Hattori A
Tsujimoto M
Source :
Journal of biochemistry [J Biochem] 2013 Sep; Vol. 154 (3), pp. 219-28. Date of Electronic Publication: 2013 Aug 14.
Publication Year :
2013

Abstract

The human endoplasmic reticulum aminopeptidase (ERAP) 1 and 2 proteins were initially identified as homologues of human placental leucine aminopeptidase/insulin-regulated aminopeptidase. They are categorized as a unique class of proteases based on their subcellular localization on the luminal side of the endoplasmic reticulum. ERAPs play an important role in the N-terminal processing of the antigenic precursors that are presented on the major histocompatibility complex (MHC) class I molecules. ERAPs are also implicated in the regulation of a wide variety of physiological phenomena and pathogenic conditions. In this review, the current knowledge on ERAPs is summarized.

Details

Language :
English
ISSN :
1756-2651
Volume :
154
Issue :
3
Database :
MEDLINE
Journal :
Journal of biochemistry
Publication Type :
Academic Journal
Accession number :
23946506
Full Text :
https://doi.org/10.1093/jb/mvt066