Passer au contenu principal

endoplasmic reticulum aminopeptidase 1

The ERAP1 gene  provides instructions for making a protein called endoplasmic reticulum aminopeptidase 1. As its name suggests, this protein is active in a cellular structure called the endoplasmic reticulum, which is involved in protein processing and transport. This protein is an aminopeptidase, which is an enzyme that cuts (cleaves) other proteins into smaller fragments called peptides.

Normal function

The ERAP1 gene  provides instructions for making a protein called endoplasmic reticulum aminopeptidase 1. As its name suggests, this protein is active in a cellular structure called the endoplasmic reticulum, which is involved in protein processing and transport. This protein is an aminopeptidase, which is an enzyme that cuts (cleaves) other proteins into smaller fragments called peptides.

Endoplasmic reticulum aminopeptidase 1 has two major functions, both of which are important for normal immune system function. First, the protein cleaves several other proteins called cytokine receptors on the surface of cells. Cleaving these receptors reduces their ability to transmit chemical signals into the cell, which affects the process of inflammation.

Second, endoplasmic reticulum aminopeptidase 1 cleaves many types of proteins into small peptides that can be recognized by the immune system.  These peptides are exported to the cell surface, where they attach to major histocompatibility complex (MHC) class I proteins.  MHC class I proteins display the peptides to the immune system. If the immune system recognizes the peptides as foreign (such as viral or bacterial peptides), it responds by triggering the infected cell to self-destruct.

While the protein is involved in the normal functioning of the immune system, it plays a particular role in protecting the body against the development of autoimmune disorders and cancer.

Conditions referring to this gene or chromosome

Other names

A-LAP

adipocyte-derived leucine aminopeptidase

ALAP

aminopeptidase PILS

aminopeptidase regulator of TNFR1 shedding

APPILS

ARTS-1

ARTS1

ERAAP

ERAAP1

ERAP1_HUMAN

KIAA0525

PILS-AP

PILSAP

puromycin-insensitive leucyl-specific aminopeptidase

type 1 tumour necrosis factor receptor shedding aminopeptidase regulator

Related patient information and medicines

Dépistage du syndrome de Down

Patient information leaflet

Dépistage du syndrome de Down

This is known as trisomy 21 (trisomy means there are three copies of. Because there is an extra chromosome 21, there is extra genetic material in the body. This causes the typical features of Syndrome de Down. See the separate leaflet called Down's syndrome for more details. What increases your chance of having a baby with Down's syndrome. Anyone.

Maladie de Wilson

Patient information leaflet

Maladie de Wilson

Maladie de Wilson is a genetic disorder in which copper builds up in the body, mainly in the foie and brain. Without any treatment, the build-up of copper can cause serious symptoms. Treatment is with medication to remove the excess copper and/or to prevent a further build-up of copper. What is Wilson's disease. Wilson's disease is a condition.

Trait drépanocytaire

Patient information leaflet

Trait drépanocytaire

If you inherit a gene from one of your parents, called a sickle cell gene, you have a condition called sickle cell trait. If you inherit a sickle cell gene from both parents, you get a double dose of the sickle cell gene. This causes a condition called sickle cell disease (SCD). What is sickle cell trait. Sickle cell trait means having one gene.

Syndrome de Gilbert

Patient information leaflet

Syndrome de Gilbert

Gilbert's syndrome is due to an inherited defect in processing bilirubin in the liver. Bilirubin is produced from the breakdown of red blood cells. When it cannot be cleared properly in the liver, its levels build up in the blood. This can cause mild jaundice from time to time and can also be seen as slightly raised bilirubin levels on a blood.

Hémochromatose

Patient information leaflet

Hémochromatose

Arthritis fou... The need for treatment to remove excess iron does not depend on the presence of symptoms. Because of the risk of developing a serious complication such as cirrhosis, treatment to remove iron buildup from the body is very important even if there are no symptoms. Causes of haemochromatosis Haemochromatosis is a genetic condition. It.

Hémophilie

Patient information leaflet

Hémophilie

The vast majority of cases sont inherited, so people are usually born with the condition. Both haemophilias sont hérité comme X-linked recessive conditions. This describes how the abnormal haemophilia gene is passed from parent to child. Genes and haemophilia In the centre (nucleus) of most cells in your body, the DNA molecule is packaged into.

Lectures complémentaires et références

Historique de l'article

Les informations sur cette page sont rédigées et examinées par des cliniciens qualifiés.
  • 23 mars 2022 | Dernière version
  • 1 mars 2022 | Publié à l'origine

Participez à la conversation

Partagez vos pensées ou expériences avec les autres dans notre communautés de patients.

Avertissement : The views expressed in the community do not represent medical advice. For any health concerns, consult your GP or healthcare provider.
vérificateur d'éligibilité à la grippe

Demandez, partagez, connectez-vous.

Parcourez les discussions, posez des questions et partagez vos expériences sur des centaines de sujets de santé.

Inscrivez-vous à la newsletter Patient

Votre dose hebdomadaire de conseils de santé clairs et fiables - rédigés pour vous aider à vous sentir informé, confiant et maître de la situation.

Veuillez entrer une adresse e-mail valide

En vous abonnant, vous acceptez notre Politique de confidentialité. Vous pouvez vous désabonner à tout moment. Nous ne vendons jamais vos données.