996 resultados para ddc: 378.2


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Leukotriene A4 (LTA4) hydrolase [(7E,9E,11Z,14Z)-(5S,6S)-5,6-epoxyicosa-7, 9,11,14-tetraenoate hydrolase; EC 3.3.2.6] is a bifunctional zinc metalloenzyme that catalyzes the final step in the biosynthesis of the potent chemotactic agent leukotriene B4 (LTB4). LTA4 hydrolase/aminopeptidase is suicide inactivated during catalysis via an apparently mechanism-based irreversible binding of LTA4 to the protein in a 1:1 stoichiometry. Previously, we have identified a henicosapeptide, encompassing residues Leu-365 to Lys-385 in human LTA4 hydrolase, which contains a site involved in the covalent binding of LTA4 to the native enzyme. To investigate the role of Tyr-378, a potential candidate for this binding site, we exchanged Tyr for Phe or Gln in two separate mutants. In addition, each of two adjacent and potentially reactive residues, Ser-379 and Ser-380, were exchanged for Ala. The mutated enzymes were expressed as (His)6-tagged fusion proteins in Escherichia coli, purified to apparent homogeneity, and characterized. Enzyme activity determinations and differential peptide mapping, before and after repeated exposure to LTA4, revealed that wild-type enzyme and the mutants [S379A] and [S380A]LTA4hydrolase were equally susceptible to suicide inactivation whereas the mutants in position 378 were no longer inactivated or covalently modified by LTA4. Furthermore, in [Y378F]LTA4 hydrolase, the value of kcat for epoxide hydrolysis was increased 2.5-fold over that of the wild-type enzyme. Thus, by a single-point mutation in LTA4 hydrolase, catalysis and covalent modification/inactivation have been dissociated, yielding an enzyme with increased turnover and resistance to mechanism-based inactivation.

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This layer is a georeferenced raster image of the historic paper map entitled: Nova Helvetiae tabula geographica : illustrissimis et potentissimis cantonibus et rebuspublicis reformatae religionis Tigurinae, Bernensi, Glaronensi, Basiliensi, Scaphusianae, Abbatis Cellanae, dominis suis clementissimis humillime [de]dicata a Ioh. Iacobo Scheuchzero Tigurino med. d. math. prof. It was published by ex officin â Petri Schenkii, in platea vulgo de Warmoesstraat sub signo N. Visschers Athlas ca. 1715. Covers Switzerland. Scale [ca. 1:378,000]. This layer is image 2 of 4 total images of the four sheet source map, representing the southwest portion of the map. Map in Latin and Dutch.The image inside the map neatline is georeferenced to the surface of the earth and fit to the Europe Lambert Conformal Conic coordinate system. All map collar and inset information is also available as part of the raster image, including any inset maps, profiles, statistical tables, directories, text, illustrations, index maps, legends, or other information associated with the principal map. This map shows features such as drainage, cities and other human settlements, territorial and administrative boundaries, roads, and more. Relief shown pictorially. Includes also illustrations. This layer is part of a selection of digitally scanned and georeferenced historic maps from the Harvard Map Collection. These maps typically portray both natural and manmade features. The selection represents a range of originators, ground condition dates, scales, and map purposes.

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Stable isotopic and micropaleontological studies were made of selected sapropels (organic-rich sediments) deposited in the Mediterranean Sea during the last 5.0 m.y. to determine the processes responsible for their formation. Distinct isotopic and faunal changes occur across sapropels of late Pleistocene, early Pleistocene and latest Pliocene age, while smaller isotopic changes and more stable faunal assemblages are associated with the early and mid-late Pliocene sapropels. The large d18O depletions and euryhaline fauna associated with latest Pliocene-Pleistocene sapropels supports a density stratification model with a low salinity surface layer. In contrast, early Pliocene and mid-late Pliocene sapropels appear to have been formed as the result of sluggish circulation and low oxygen contents in bottom waters of the eastern Mediterranean due to the stable, warm climatic conditions of that time period.

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National Highway Safety Bureau, Washington, D.C.

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The increasing prevalence, variable pathogenesis, progressive natural history, and complications of type 2 diabetes emphasise the urgent need for new treatment strategies. Longacting (eg, once weekly) agonists of the glucagon-like-peptide-1 receptor are advanced in development, and they improve prandial insulin secretion, reduce excess glucagon production, and promote satiety. Trials of inhibitors of dipeptidyl peptidase 4, which enhance the effect of endogenous incretin hormones, are also nearing completion. Novel approaches to glycaemic regulation include use of inhibitors of the sodium-glucose cotransporter 2, which increase renal glucose elimination, and inhibitors of 11ß-hydroxysteroid dehydrogenase 1, which reduce the glucocorticoid effects in liver and fat. Insulin-releasing glucokinase activators and pancreatic-G-protein-coupled fatty-acid-receptor agonists, glucagon-receptor antagonists, and metabolic inhibitors of hepatic glucose output are being assessed. Early proof of principle has been shown for compounds that enhance and partly mimic insulin action and replicate some effects of bariatric surgery.

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