4.2 Review

Endoplasmic reticulum aminopeptidases: biochemistry, physiology and pathology

Journal

JOURNAL OF BIOCHEMISTRY
Volume 154, Issue 3, Pages 219-228

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jb/mvt066

Keywords

aminopeptidase; ankylosis spondylitis; antigen presentation; autoimmune diseases; endoplasmic reticulum

Funding

  1. Japan Society for the Promotion of Science
  2. Ministry of Education, Culture, Sports, Science and Technology of Japan
  3. Grants-in-Aid for Scientific Research [25293083, 23310160, 24659153, 24659099] Funding Source: KAKEN

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available