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ho·mo·car·no·sine (ho″mo-kahrґno-sēn) a dipeptide consisting of γ-aminobutyric acid and histidine, found in the brain.Medical dictionary. 2011.
Carnosinemia — Infobox Disease Name = PAGENAME Caption = Carnosine DiseasesDB = 29672 ICD10 = ICD10|E|70|8|e|70 ICD9 = ICD9|270.5 ICDO = OMIM = 212200 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = Carnosinemia, also called carnosinase… … Wikipedia
Carnosine — Chembox new Reference= [ [http://www.sigmaaldrich.com/catalog/search/ProductDetail/SIGMA/C9625 Carnosine] at Sigma Aldrich] ImageFile=Carnosine.png ImageSize=200px IUPACName=(2 S ) 2 [(3 Amino 1 oxopropyl)amino] 3 (3 H imidazol 4 yl)propanoic… … Wikipedia
Carnosina — Saltar a navegación, búsqueda Carnosina Nombre (IUPAC) sistemático ácido propanoico (2S) 2 [(3 amino 1 oxopropil)amino] 3 (3H i … Wikipedia Español
Карнозин — Общие … Википедия
Carnosine synthase — In enzymology, a carnosine synthase (EC number|6.3.2.11) is an enzyme that catalyzes the chemical reaction:ATP + L histidine + beta alanine ightleftharpoons AMP + diphosphate + carnosineThe 3 substrates of this enzyme are ATP, L histidine, and… … Wikipedia
homocarnosinosis — An inborn error in metabolism in which homocarnosine levels are elevated, particularly in the cerebral spinal fluid. * * * ho·mo·car·no·sin·o·sis (ho″mo kahr″no sĭ noґsis) an autosomal recessive aminoacidopathy characterized by… … Medical dictionary
X-His dipeptidase — X His di·pep·ti·dase (di pepґtĭ dās) [EC 3.4.13.3] an enzyme of the hydrolase class that catalyzes the cleavage of the dipeptide carnosine into component amino acids β alanine and histidine; it also acts on some other aminoacyl L… … Medical dictionary
CNDP1 — Carnosine dipeptidase 1 (metallopeptidase M20 family), also known as CNDP1, is a human gene.cite web | title = Entrez Gene: CNDP1 carnosine dipeptidase 1 (metallopeptidase M20 family)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
4-aminobutyrate transaminase — 4 ami·no·bu·ty·rate trans·am·i·nase (ə me″no buґtə rāt trans amґĭ nās) [EC 2.6.1.19] an enzyme of the transferase class that catalyzes the transfer of an amino group from γ aminobutyrate (GABA) to α… … Medical dictionary
serum carnosinase deficiency — an autosomal recessive aminoacidopathy of carnosine metabolism, due to deficiency of the serum isozyme of X His dipeptidase; it is characterized by urinary excretion of carnosine and accumulation of homocarnosine in the cerebrospinal fluid and… … Medical dictionary
