ACE2: from vasopeptidase to SARS virus receptor.
Identifieur interne : 002E48 ( PubMed/Checkpoint ); précédent : 002E47; suivant : 002E49ACE2: from vasopeptidase to SARS virus receptor.
Auteurs : Anthony J. Turner [Royaume-Uni] ; Julian A. Hiscox ; Nigel M. HooperSource :
- Trends in pharmacological sciences [ 0165-6147 ] ; 2004.
Descripteurs français
- KwdFr :
- Animaux, Hormones peptidiques (métabolisme), Hormones peptidiques (physiologie), Humains, Isoenzymes (génétique), Isoenzymes (physiologie), Peptide hydrolases (physiologie), Peptidyl-Dipeptidase A (génétique), Peptidyl-Dipeptidase A (physiologie), Récepteurs viraux (génétique), Vaisseaux sanguins (métabolisme), Vaisseaux sanguins (physiologie), Virus du SRAS (génétique).
- MESH :
- génétique : Isoenzymes, Peptidyl-Dipeptidase A, Récepteurs viraux, Virus du SRAS.
- métabolisme : Hormones peptidiques, Vaisseaux sanguins.
- physiologie : Hormones peptidiques, Isoenzymes, Peptide hydrolases, Peptidyl-Dipeptidase A, Vaisseaux sanguins.
- Animaux, Humains.
English descriptors
- KwdEn :
- Animals, Blood Vessels (metabolism), Blood Vessels (physiology), Humans, Isoenzymes (genetics), Isoenzymes (physiology), Peptide Hormones (metabolism), Peptide Hormones (physiology), Peptide Hydrolases (physiology), Peptidyl-Dipeptidase A (genetics), Peptidyl-Dipeptidase A (physiology), Receptors, Virus (genetics), SARS Virus (genetics).
- MESH :
- chemical , genetics : Isoenzymes, Peptidyl-Dipeptidase A, Receptors, Virus.
- genetics : SARS Virus.
- metabolism : Blood Vessels, Peptide Hormones.
- physiology : Blood Vessels, Isoenzymes, Peptide Hormones, Peptide Hydrolases, Peptidyl-Dipeptidase A.
- Animals, Humans.
Abstract
The zinc metallopeptidase angiotensin-converting enzyme 2 (ACE2) is the only known human homologue of the key regulator of blood pressure angiotensin-converting enzyme (ACE). Since its discovery in 2000, ACE2 has been implicated in heart function, hypertension and diabetes, with its effects being mediated, in part, through its ability to convert angiotensin II to angiotensin-(1-7). Unexpectedly, ACE2 also serves as the cellular entry point for the severe acute respiratory syndrome (SARS) virus and the enzyme is therefore a prime target for pharmacological intervention on several disease fronts.
DOI: 10.1016/j.tips.2004.04.001
PubMed: 15165741
Affiliations:
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pubmed:15165741Le document en format XML
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<front><div type="abstract" xml:lang="en">The zinc metallopeptidase angiotensin-converting enzyme 2 (ACE2) is the only known human homologue of the key regulator of blood pressure angiotensin-converting enzyme (ACE). Since its discovery in 2000, ACE2 has been implicated in heart function, hypertension and diabetes, with its effects being mediated, in part, through its ability to convert angiotensin II to angiotensin-(1-7). Unexpectedly, ACE2 also serves as the cellular entry point for the severe acute respiratory syndrome (SARS) virus and the enzyme is therefore a prime target for pharmacological intervention on several disease fronts.</div>
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<Abstract><AbstractText>The zinc metallopeptidase angiotensin-converting enzyme 2 (ACE2) is the only known human homologue of the key regulator of blood pressure angiotensin-converting enzyme (ACE). Since its discovery in 2000, ACE2 has been implicated in heart function, hypertension and diabetes, with its effects being mediated, in part, through its ability to convert angiotensin II to angiotensin-(1-7). Unexpectedly, ACE2 also serves as the cellular entry point for the severe acute respiratory syndrome (SARS) virus and the enzyme is therefore a prime target for pharmacological intervention on several disease fronts.</AbstractText>
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