enoyl-acyl protein reductase

enoyl-acyl protein reductase
енол-ацил протеин редуктаза
фермент бактерий, участвующий в синтезе жирных кислот

English-Russian Biotechnology Glossary. . 2007.

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  • Enoyl-acyl carrier protein reductase — (or ENR) (EC number|1.3.1.9), is a key enzyme of the type II fatty acid synthesis (FAS) system. (PMID 15139852) ENR is an attractive target for narrow spectrum antibacterial drug discovery because of its essential role in metabolism and its… …   Wikipedia

  • Enoyl-(acyl-carrier-protein) reductase (NADPH, B-specific) — In enzymology, an enoyl [acyl carrier protein] reductase (NADPH, B specific) (EC number|1.3.1.10) is an enzyme that catalyzes the chemical reaction:acyl [acyl carrier protein] + NADP+ ightleftharpoons trans 2,3 dehydroacyl [acyl carrier protein]… …   Wikipedia

  • Enoyl-(acyl-carrier-protein) reductase (NADPH, A-specific) — In enzymology, an enoyl [acyl carrier protein] reductase (NADPH, A specific) (EC number|1.3.1.39) is an enzyme that catalyzes the chemical reaction:acyl [acyl carrier protein] + NADP+ ightleftharpoons trans 2,3 dehydroacyl [acyl carrier protein]… …   Wikipedia

  • enoyl-ACP reductase — An enzyme catalyzing hydrogenation of acyl ACP (where ACP is acyl carrier protein) complexes to 2,3 dehydroacyl ACP s, with NAD+ as hydrogen acceptor; important in fatty acid metabolism. SYN: crotonyl ACP reductase. An …   Medical dictionary

  • 7-Dehydrocholesterol reductase — Identifiers Symbols DHCR7; SLOS External IDs OMIM …   Wikipedia

  • Mitochondrial trifunctional protein — Schematic demonstrating mitochondrial fatty acid beta oxidation and effects of long chain 3 hydroxyacyl coenzyme A dehydrogenase deficiency, LCHAD deficiency Mitochondrial trifunctional protein is a protein which catalyzes several reactions in… …   Wikipedia

  • Mitochondrial trifunctional protein deficiency — Classification and external resources OMIM 609015 DiseasesDB 34111 eMedi …   Wikipedia

  • D-Bifunctional Protein Deficiency — (officially called 17 β hydroxysteroid dehydrogenase) is an autosomal recessive peroxisomal fatty acid oxidation disorder. Peroxisomal disorders are usually caused by a combination of peroxisomal assembly defects or by deficiencies of specific… …   Wikipedia

  • D-bifunctional protein deficiency — Classification and external resources ICD 10 E80.3 OMIM 261515 DiseasesDB …   Wikipedia

  • енол-ацил протеин редуктаза — Фермент бактерий, участвующий в синтезе жирных кислот [http://www.dunwoodypress.com/148/PDF/Biotech Eng Rus.pdf] Тематики биотехнологии EN enoyl acyl protein reductase …   Справочник технического переводчика

  • List of EC numbers (EC 1) — This list contains a list of EC numbers for the first group, EC 1, oxidoreducatases, placed in numerical order as determined by the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology.EC 1.1 Acting on the CH OH …   Wikipedia


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