نتایج جستجو برای: kinetic inhibitor

تعداد نتایج: 295228  

2013
Sudipta Sen Arindam Chatterjee Debanjan Sarkar

Journal: :The Biochemical journal 1986
B Mannervik I Jakobson M Warholm

Optimal design of experiments as well as proper analysis of data are dependent on knowledge of the experimental error. A detailed analysis of the error structure of kinetic data obtained with acetylcholinesterase showed conclusively that the classical assumptions of constant absolute or constant relative error are inadequate for the dependent variable (velocity). The best mathematical models fo...

2017
Mike Sleutel Imke Van den Broeck Nani Van Gerven Cécile Feuillie Wim Jonckheere Claire Valotteau Yves F Dufrêne Han Remaut

Curli are functional amyloids produced by proteobacteria like Escherichia coli as part of the extracellular matrix that holds cells together into biofilms. The molecular events that occur during curli nucleation and fiber extension remain largely unknown. Combining observations from curli amyloidogenesis in bulk solutions with real-time in situ nanoscopic imaging at the single-fiber level, we s...

2007
J. L. Zhang H. Rusinek L. Bokacheva Q. Chen P. Storey C. Prince V. S. Lee

Dynamic contrast-enhanced MR renography, analyzed with appropriate tracer kinetic models [1], is a promising technique for the non-invasive assessment of glomerular filtration rate (GFR). Dual-injection measurements, such as before and after administration of an angiotensin-convertingenzyme (ACE) inhibitor, have been proposed as an improved diagnostic marker of renovascular disease [2]. Technic...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1997
S K Thompson S M Halbert M J Bossard T A Tomaszek M A Levy B Zhao W W Smith S S Abdel-Meguid C A Janson K J D'Alessio M S McQueney B Y Amegadzie C R Hanning R L DesJarlais J Briand S K Sarkar M J Huddleston C F Ijames S A Carr K T Garnes A Shu J R Heys J Bradbeer D Zembryki L Lee-Rykaczewski I E James M W Lark F H Drake M Gowen J G Gleason D F Veber

Potent and selective active-site-spanning inhibitors have been designed for cathepsin K, a cysteine protease unique to osteoclasts. They act by mechanisms that involve tight binding intermediates, potentially on a hydrolytic pathway. X-ray crystallographic, MS, NMR spectroscopic, and kinetic studies of the mechanisms of inhibition indicate that different intermediates or transition states are b...

2010
Helge C. Dorfmueller Daan M.F. van Aalten

O-GlcNAcylation is an essential posttranslational modification in metazoa. Modulation of O-GlcNAc levels with small molecule inhibitors of O-GlcNAc hydrolase (OGA) is a useful strategy to probe the role of this modification in a range of cellular processes. Here we report the discovery of novel, low molecular weight and drug-like O-GlcNAcase inhibitor scaffolds by high-throughput screening. Kin...

Journal: :Antimicrobial agents and chemotherapy 2004
Laurent Poirel Hedi Mammeri Patrice Nordmann

Enterobacter aerogenes clinical isolate LOR was resistant to penicillins and ceftazidime but susceptible to cefuroxime, cephalothin, cefoxitin, cefotaxime, ceftriaxone, and cefepime. PCR and cloning experiments from this strain identified a novel TEM-type beta-lactamase (TEM-121) differing by five amino acid substitutions from beta-lactamase TEM-2 (Glu104Lys, Arg164Ser, Ala237Thr, Glu240Lys, an...

2013
Refat M. Hassan Ishaq A. Zaafarany

Corrosion inhibition of aluminum (Al) in hydrochloric acid by anionic polyeletrolyte pectates (PEC) as a water-soluble natural polymer polysaccharide has been studied using both gasometric and weight loss techniques. The results drawn from these two techniques are comparable and exhibit negligible differences. The inhibition efficiency was found to increase with increasing inhibitor concentrati...

Journal: :The Journal of biological chemistry 1972
C D Ashby D A Walsh

The interaction of a protein inhibitor with the catalytic subunit derived from adenosine 3’,5’-monophosphatedependent protein kinase is described. A kinetic analysis of casein phosphorylation in the presence of inhibitor reveals a noncompetitive interaction between the inhibitor and the catalytic subunit substrates, ATP and casein. The inhibitor does not function by destroying ATP nor by acting...

Journal: :The Journal of biological chemistry 1989
D Serra G Asins V E Calvet F G Hegardt

A heat-stable protein inhibitor of the hydroxymethylglutaryl-CoA reductase phosphatase 2A activity has been identified and purified to homogeneity, as judged by polyacrylamide gel electrophoresis. The apparent molecular mass was 20,000 Da. The protein lost its inhibitory properties when incubated with trypsin or treated with ethanol. The inhibitor protein does not inhibit type 1 phosphatase whe...

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