Carnitine O-palmitoyltransferase
- Carnitine O-palmitoyltransferase
Carnitine O-palmitoyltransferase (also called carnitine palmitoyltransferase or carnitine acyltransferase) is a mitochondrial transferase enzyme (EC number|2.3.1.21) involved in the metabolism of palmitoylcarnitine into palmitoyl-CoA.
Molecules
Pathway
Human forms of CPT
There are four different forms of CPT in humans:
* CPT1A - associated with Carnitine palmitoyltransferase I deficiency
* CPT1B
* CPT1C
* CPT2 - associated with Carnitine palmitoyltransferase II deficiency
ee also
* Fatty_acid_degradation#Transport_into_the_mitochondrial_matrix
External links
* - Acyltransferases ChoActase / COT / CPT family in PROSITE
* [http://pfam.sanger.ac.uk/family?entry=PF00755 Choline/Carnitine o-acyltransferase family] in Pfam
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Look at other dictionaries:
Carnitine O-palmitoyltransférase — La carnitine O palmitoyltransférase (CPT) est une enzyme mitochondriale de type transférase (EC 2.3.1.21), impliquée dans le métabolisme de la palmitoylcarnitine en palmitoyl CoA. Une enzyme transférase proche est la carnitine acyltransférase.… … Wikipédia en Français
carnitine O-palmitoyltransferase — car·ni·tine O pal·mi·to·yl·trans·fer·ase (kahrґnĭ tēn pahl″mĭ to″əl transґfər ās) [EC 2.3.1.21] an enzyme of the transferase class that catalyzes the transfer between coenzyme A and carnitine of long… … Medical dictionary
Carnitine palmitoyltransferase I — carnitine palmitoyltransferase 1A (liver) Identifiers Symbol CPT1A Alt. symbols CPT1 Entrez 1374 … Wikipedia
carnitine acyltransferase — car·ni·tine ac·yl·trans·fer·ase (kahrґnĭ tēn a″səl transґfər ās) carnitine O palmitoyltransferase … Medical dictionary
Carnitine palmitoyltransferase II deficiency — Classification and external resources Carnitine ICD 9 … Wikipedia
Carnitine palmitoyltransferase II — Carnitine palmitoyltransferase II, also known as CPT2, is a human gene.cite web | title = Entrez Gene: CPT2 carnitine palmitoyltransferase II| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=1376| accessdate … Wikipedia
Carnitine — Systematic (IUPAC) name 3 hydroxy 4 (trimethylazaniumyl)butanoate Clinical data AHFS/Drugs.com … Wikipedia
Carnitine palmitoyltransferase I deficiency — Infobox Disease Name = PAGENAME Caption = Carnitine DiseasesDB = 32535 ICD10 = ICD9 = ICD9|277.85 ICDO = OMIM = 255120 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 321 MeshName = MeshNumber = Carnitine palmitoyltransferase I deficiency is a … Wikipedia
Carnitine-acylcarnitine translocase deficiency — DiseaseDisorder infobox Name = Carnitine acylcarnitine translocase deficiency ICD10 = ICD9 = ICD9|272.8 Carnitine acylcarnitine translocase deficiency is a rare, autosomal recessive metabolic disorder that prevents the body from converting long… … Wikipedia
Carnitine O-octanoyltransferase — In enzymology, a carnitine O octanoyltransferase (EC number|2.3.1.137) is an enzyme that catalyzes the chemical reaction:octanoyl CoA + L carnitine ightleftharpoons CoA + L octanoylcarnitineThus, the two substrates of this enzyme are octanoyl CoA … Wikipedia
