Angiotensin Converting Enzyme 1 est un gène codé par le symbole ACE. D'autres noms incluent: Angiotensin-converting enzyme; ACE; Dipeptidyl carboxypeptidase I; Kininase II; DCP; DCP1. Angiotensin Converting Enzyme 1 a une masse de 149.72kDa, une longueur d'acide aminé de 1306, et est impliqué dans les maladies: Ischemic stroke; Renal tubular dysgenesis; Microvascular complications of diabetes 3; Intracerebral hemorrhage.
Nous proposons 19 Angiotensin Converting Enzyme 1 kits ELISA pour la détection qualitative ou quantitative de Angiotensin Converting Enzyme 1 à partir d'échantillons Humain, Souris, Rat, Bovin, Porcin, Lapin, Singe, Mouton et Cochon d'Inde.
Informations sur les Gènes et les Protéines
Résumé UniProt
Converts angiotensin I to angiotensin II by release of the terminal His-Leu, this results in an increase of the vasoconstrictor activity of angiotensin. Also able to inactivate bradykinin, a potent vasodilator. Has also a glycosidase activity which releases GPI-anchored proteins from the membrane by cleaving the mannose linkage in the GPI moiety.
Résumé Entrez
This gene encodes an enzyme involved in catalyzing the conversion of angiotensin I into a physiologically active peptide angiotensin II. Angiotensin II is a potent vasopressor and aldosterone-stimulating peptide that controls blood pressure and fluid-electrolyte balance. This enzyme plays a key role in the renin-angiotensin system. Many studies have associated the presence or absence of a 287 bp Alu repeat element in this gene with the levels of circulating enzyme or cardiovascular pathophysiologies. Multiple alternatively spliced transcript variants encoding different isoforms have been identified, and two most abundant spliced variants encode the somatic form and the testicular form, respectively, that are equally active.
Spécificité tissulaire
Ubiquitously expressed, with highest levels in lung, kidney, heart, gastrointestinal system and prostate. Isoform Testis-specific is expressed in spermatocytes and adult testis.
Implication dans la maladie
Ischemic stroke: A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors.
Renal tubular dysgenesis: Autosomal recessive severe disorder of renal tubular development characterized by persistent fetal anuria and perinatal death, probably due to pulmonary hypoplasia from early-onset oligohydramnios (the Potter phenotype).
Microvascular complications of diabetes 3: Pathological conditions that develop in numerous tissues and organs as a consequence of diabetes mellitus. They include diabetic retinopathy, diabetic nephropathy leading to end-stage renal disease, and diabetic neuropathy. Diabetic retinopathy remains the major cause of new-onset blindness among diabetic adults. It is characterized by vascular permeability and increased tissue ischemia and angiogenesis.
Intracerebral hemorrhage: A pathological condition characterized by bleeding into one or both cerebral hemispheres including the basal ganglia and the cerebral cortex. It is often associated with hypertension and craniocerebral trauma. Intracerebral bleeding is a common cause of stroke.
Similitudes de séquence
Belongs to the peptidase M2 family.
Modification post-traductionnelle
Phosphorylated by CK2 on Ser-1299; which allows membrane retention.
Localisation cellulaire
Secreted.