نتایج جستجو برای: b ketoacyl coa synthase

تعداد نتایج: 993892  

Journal: :Biochemical Society transactions 2001
N Latruffe M Cherkaoui Malki V Nicolas-Frances B Jannin M C Clemencet F Hansmannel P Passilly-Degrace J P Berlot

The enzymes required for the beta-oxidation of fatty acyl-CoA are present in peroxisomes and mitochondria. Administration of hypolipidaemic compounds such as clofibrate to rodents leads to an increase in the volume and density of peroxisomes in liver cells. These proliferators also induce simultaneously the expression of genes encoding acyl-CoA oxidase, enoyl-CoA hydratase-hydroxyacyl-CoA dehyd...

Objective(s):Higher cellular reactive oxygen species (ROS) levels is important in reducing cellular energy charge (EC) by increasing the levels of key metabolic protein, and nitrosative modifications, and have been shown to damage the cardiac tissue of diabetic mice. However, the relation between energy production and heart function is unclear. Materials and Methods:Streptozotocin (STZ, 150 mg...

Journal: :Acta Crystallographica Section A Foundations of Crystallography 2006

2011
Matthew D. Hirschey Tadahiro Shimazu John A. Capra Katherine S. Pollard Eric Verdin

SIRT1 and SIRT3 are NAD+-dependent protein deacetylases that are evolutionarily conserved across mammals. These proteins are located in the cytoplasm/nucleus and mitochondria, respectively. Previous reports demonstrated that human SIRT1 deacetylates Acetyl-CoA Synthase 1 (AceCS1) in the cytoplasm, whereas SIRT3 deacetylates the homologous Acetyl-CoA Synthase 2 (AceCS2) in the mitochondria. We r...

Journal: :The Journal of infectious diseases 2011
Lee F Peng Esperance A K Schaefer Nicole Maloof Andrew Skaff Andrew Berical Craig A Belon Julie A Heck Wenyu Lin David N Frick Todd M Allen Henry M Miziorko Stuart L Schreiber Raymond T Chung

BACKGROUND Hepatitis C virus (HCV) chronically infects >170 million persons worldwide and is a leading cause of cirrhosis and hepatocellular carcinoma. The identification of more effective and better-tolerated agents for treating HCV is a high priority. We have reported elsewhere the discovery of the anti-HCV compound ceestatin using a high-throughput screen of a small molecule library. METHO...

Journal: :Journal of Biological Chemistry 2002

Journal: :Genetics 2004
Yong-Qiang Zhang Matthias Brock Nancy P Keller

Propionyl-CoA is an intermediate metabolite produced through a variety of pathways including thioesterification of propionate and catabolism of odd chain fatty acids and select amino acids. Previously, we found that disruption of the methylcitrate synthase gene, mcsA, which blocks propionyl-CoA utilization, as well as growth on propionate impaired production of several polyketides-molecules typ...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2004
Thomas Götz Peter Böger

The first elongation step to form very-long-chain fatty acids (VLCFAs) is catalyzed by the VLCFA-synthase. CoA-activated fatty acids react with malonyl-CoA to condense a C2-unit. As shown with recombinant enzyme this reaction is specifically inhibited by chloroacetamide herbicides. The inhibition is alleviated when the inhibitor (e.g. metazachlor) is incubated together with adequate concentrati...

1997
Akira Honda Gerald Salen Lien B. Nguyen G. Stephen Tint Ashok K. Batta Sarah Shefer

Sitosterolemia is a recessively inherited disorder characterized by abnormally increased plasma and tissue plant sterol concentrations. Patients have markedly reduced whole body cholesterol biosynthesis associated with suppressed hepatic, ileal, and mononuclear leukocyte 3-hydroxy3-methylglutaryl coenzyme A (HMG-CoA) reductase, the ratecontrolling enzyme in cholesterol biosynthetic pathway, cou...

Journal: :Toxicological sciences : an official journal of the Society of Toxicology 2007
Yin Guo Robert A Jolly Bartley W Halstead Thomas K Baker John P Stutz Melanie Huffman John N Calley Adam West Hong Gao George H Searfoss Shuyu Li Armando R Irizarry Hui-Rong Qian James L Stevens Timothy P Ryan

Marked species-specific responses to agonists of the peroxisome proliferator-activated alpha receptor (PPAR alpha) have been observed in rats and dogs, two species typically used to assess the potential human risk of pharmaceuticals in development. In this study, we used primary cultured rat and dog hepatocytes to investigate the underlying mechanisms of a novel PPAR alpha and -gamma coagonist,...

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