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10 Possible Causes for Acetyl CoA, Arylamine, N Acetyltransferase

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  • Mycobacterium Tuberculosis

    2009, 418 (2) 369-378; DOI: 10.1042/BJ20082011 Abstract In Mycobacterium tuberculosis , the genes hsaD (2-hydroxy-6-oxo-6-phenylhexa-2,4-dienoic acid hydrolase) and nat (arylamine[biochemj.org] […] to 4-methyl-5-oxo-octanedioyl-CoA (MOODA-CoA) and acetyl-CoA with high specificity ( k cat / K m 5.8 0.8 10 4 M -1 s -1 ).[ncbi.nlm.nih.gov] As propionyl-CoA is a product of cholesterol catabolism, we propose that NAT could have a role in the utilization of this important cofactor. arylamine N-acetyltransferase[biochemj.org]

  • Mycobacterium Smegmatis

    Arylamine N-acetyltransferase is an enzyme that is conserved in most Mycobacterium spp.[ncbi.nlm.nih.gov] (PTA)-mediated conversion of acetyl-phosphate to acetyl-CoA; (ii) acetyl-CoA synthetase (ACS)-mediated 1 conversion of acetate to acetyl-CoA through an acetyl-AMP intermediate[mcponline.org] Abstract MSMEG_0307 is annotated as a transcriptional regulator belonging to the AraC protein family and is located adjacent to the arylamine N-acetyltransferase (nat) gene[ncbi.nlm.nih.gov]

  • Cytosolic Acetoacetyl-CoA Thiolase Deficiency

    […] amidinotransferase Deficiency of amidophosphoribosyltransferase Deficiency of amine oxidase Deficiency of amine oxidase Deficiency of aryl sulfotransferase Deficiency of arylamine[icdlist.com] CoA Thiolase, Acetoacetyl; C- Acetyltransferase, Acetyl- CoA; Acetyltransferase, Acetyl- CoA; Acetyl CoA C Acetyltransferase; Acetyl CoA Acetyltransferase Substance CAS Registry[reference.md] Deficiency of transferase Disorder of branched-chain amino acid metabolism Name: Deficiency of acetyl-CoA acetyltransferase See more descriptions. - Acetoacetyl-CoA thiolase[snomedbrowser.com]

  • Acetyl-CoA Carboxylase Deficiency

    Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase Deficiency of arylamine[icd9data.com] Each monomer is composed of an all-helical N-Terminal domain and a very precise catalytic C-Terminal domain present in GCN5-Histone acetyltransferase (GNAT) family.[ddd.uab.cat] An important gene associated with Acetyl-Coa Carboxylase Deficiency is ACACA (Acetyl-CoA Carboxylase Alpha).[malacards.org]

  • Deficiency of Glycerol Kinase

    Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase Deficiency of arylamine[icd9data.com] SGSH 17q25.3 Mucopolysaccharidose IIIC (Sanfilippo C) Heparan-α-Glucosaminid-N-Acetyltransferase HGSNAT 8p11.1 Mucopolysaccharidose IIIB (Sanfilippo B) α-N-Acetylglucosaminidase[de.wikibooks.org] […] pyruvate NAD CoA goes to acetyl-CoA CO2 NADH 441 What second messenger system does Gi work through?[aippg.net]

  • Beta-Ureidopropionase Deficiency

    Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase Deficiency of arylamine[icd9data.com] SGSH 17q25.3 Mucopolysaccharidose IIIC (Sanfilippo C) Heparan-α-Glucosaminid-N-Acetyltransferase HGSNAT 8p11.1 Mucopolysaccharidose IIIB (Sanfilippo B) α-N-Acetylglucosaminidase[de.wikibooks.org] Joint effects of the N-acetyltransferase 1 and 2 (NAT1 and NAT2) genes and smoking on bladder carcinogenesis: a literature-based systematic HuGE review and evidence synthesis[nature.com]

  • Aromatic L-Amino Acid Decarboxylase Deficiency

    Deficiency of amylo-1,6-glucosidase Deficiency of arginine deiminase Deficiency of aromatic-L-amino-acid decarboxylase Deficiency of aryl sulfotransferase Deficiency of arylamine[icd9data.com] Spermidine/spermine-N (1)-acetyltransferase: a key metabolic regulator. American Journal of Physiology Endocrinology and Metabolism 294(6): 995-1010.[revistas.chapingo.mx] Metabolism of the branched-chain amino acids produces acetyl-CoA and acetoacetate.[slideplayer.es]

  • Xeroderma Pigmentosum Complementation Group C

    N-Acetyltransferase)); NAT2 (N-Acetyltransferase 2 (Arylamine N-Acetyltransferase)); NB (Neuroblastom (Neuroblastom-Supressor)); NCAM1 (Neurales Zell Adhäsionsmolekül 1);[google.mk] Aarskog syndrome Acanthocytosis Acatalasemia Acetyl-CoA carboxylase deficiency Achondroplasia ACTH deficiency Acute hepatic porphyria Acute intermittent porphyria Acyl-CoA[easternbiotech.com] Anheftungsprotein, gamma); NAT1 (N-Acetyltransferase 1 (Arylamin N-Acetyltransferase)); NAT2 (N-Acetyltransferase 2 (Arylamine N-Acetyltransferase)); NB (Neuroblastom (Neuroblastom-Supressor[google.mk]

  • Atrial Standstill

    2 (arylamine N-acetyltransferase) (EC:2.3.1.5) C00001492 4942 OAT, GACR, HOGA, OATASE, OKT ornithine aminotransferase (EC:2.6.1.13) C00001492 5062 PAK2, PAK65, PAKgamma p21[genome.jp] , MAC30 transmembrane protein 97 C00001492 7292 TNFSF4, CD134L, CD252, GP34, OX-40L, OX4OL, TXGP1 tumor necrosis factor (ligand) superfamily, member 4 C00001492 39 ACAT2 acetyl-CoA[genome.jp] MTOR, FRAP, FRAP1, FRAP2, RAFT1, RAPT1 mechanistic target of rapamycin (serine/threonine kinase) (EC:2.7.11.1) C00001492 10 NAT2, AAC2, NAT-2, PNAT N-acetyltransferase 2 (arylamine[genome.jp]

  • Tacrine

    NAT2 (N-acetyltransferase 2 (arylamine N-acetyltransferase)). In: Cacabelos R (Ed). World guide for drug use and pharmacogenomics.[euroespes.com] NAT2 (N-acetyltransferase 2 (arylamine N-acetyltransferase)). In: Cacabelos R (Ed). World guide for drug use and pharmacogenomics.[euroespes.com] ACACA (acetyl-coA carboxylase alpha). In: Cacabelos R (Ed). World guide for drug use and pharmacogenomics. EuroEspes Publishing, Coruña, 2012:1026-1027.[euroespes.com]