methylmalonyl-CoA epimerase
Dernière mise à jour 1 juin 2021
Respecte les directives éditoriales
- TéléchargerTélécharger
- Partager
- Language
- Discussion
- Version audio
- Ajouter aux sources préférées sur Google
La MCEE gene provides instructions for making an enzyme called methylmalonyl CoA epimerase, which converts one form of the molecule methylmalonyl CoA to another. Specifically, the enzyme converts D-methylmalonyl CoA to L-methylmalonyl CoA. This conversion takes place within the pathway that converts the molecule propionyl-CoA to succinyl-CoA. This pathway is important in the breakdown of certain protein building blocks (amino acids), specific fats (lipids), and cholesterol.
Normal function
La MCEE gene provides instructions for making an enzyme called methylmalonyl CoA epimerase, which converts one form of the molecule methylmalonyl CoA to another. Specifically, the enzyme converts D-methylmalonyl CoA to L-methylmalonyl CoA. This conversion takes place within the pathway that converts the molecule propionyl-CoA to succinyl-CoA. This pathway is important in the breakdown of certain protein building blocks (amino acids), specific fats (lipids), and cholesterol.
Conditions referring to this gene or chromosome
Other names
DL-methylmalonyl-CoA racemase
GLOD2
glyoxalase domain containing 2
MCEE_HUMAN
methylmalonyl CoA epimerase
methylmalonyl-CoA epimerase, mitochondrial
methylmalonyl-CoA epimerase, mitochondrial precursor
Related patient information and medicines

Patient information leaflet
Coarctation de l'aorte
How common is coarctation of the aorta. Congenital heart disease occurs in about 7 dans 1,000 pregnancies and coarctation of the aorta is just one type of congenital cœur maladie. Around 1 in 2,500 babies have coarctation of the aorta. The condition is twice as common in males as it is in females and it is one of the more common congenital heart.

Medicine leaflet
Comprimés de pravastatine
Over time, these patches can make a blood vessel narrower and this is called... The narrowing reduces the blood flow through the artery and increases the risk of a number of heart and blood vessel diseases, such as heart attack and stroke. Pravastatin belongs to a group of medicines known as statins (or HMG-CoA reductase inhibitors). It reduces.

Medicine leaflet
Comprimés et capsules de fluvastatine
Fluvastatin belongs to a group of medicines known as statins. It regulates the amount of cholesterol and other lipids made by your body, and helps to reduce the risk of heart and blood vessel disease. The narrowing reduces the blood flow through the artery and increases the risk of a number of heart and blood vessel diseases, such a... Fluvastatin.

Medicine leaflet
Rosuvastatine
Rosuvastatine belongs to a group of medicines known as statins. It regulates ... About rosuvastatin Type of medicine A lipid-regulating medicine commonly known as a statin Used for Lowering cholesterol and other lipids in the blood; to reduce the risk of heart and blood vessel disease Also called Crestor® Available as Tablets and capsules Lipids,.

Medicine leaflet
Simvastatine
Simvastatine belongs to a group of medicines known as statins. À propos simvastatine Type of medicine A lipid-regulating medicine commonly known as a statin Used for Lowering cholesterol and other lipids in the blood; to reduce the risk of heart and blood vessel disease Also called Zocor®; Combination brand: Inegy® (simvastatin with ezetimibe ).

Medicine leaflet
Comprimés d'atorvastatine
À propos atorvastatine Type of medicine A lipid-regulating medicine commonly known as a statine Used for Lowering cholesterol and other lipids; to reduce the risk of heart and blood vessel disease Also called (UK) Lipitor® Also called (USA) Lipitor®; Combination brand: Caduet® (atorvastatin with amlodipine ) Available as Tablets and chewable tablets.
Lectures complémentaires et références
- methylmalonyl-CoA epimerase; MedlinePlus, National Library of Medicine.
- Bikker H, Bakker HD, Abeling NG, Poll-The BT, Kleijer WJ, Rosenblatt DS, Waterham HR, Wanders RJ, Duran M. A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria. Hum Mutat. 2006 Jul;27(7):640-3. doi: 10.1002/humu.20373.
- Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria. Mol Genet Metab. 2006 Aug;88(4):327-33. doi: 10.1016/j.ymgme.2006.03.009. Epub 2006 May 11.
- Gradinger AB, Belair C, Worgan LC, Li CD, Lavallee J, Roquis D, Watkins D, Rosenblatt DS. Atypical methylmalonic aciduria: frequency of mutations in the methylmalonyl CoA epimerase gene (MCEE). Hum Mutat. 2007 Oct;28(10):1045. doi: 10.1002/humu.9507.
Participez à la conversation
Partagez vos pensées ou expériences avec les autres dans notre communautés de patients.

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