نتایج جستجو برای: methionine sulfoxide reductase

تعداد نتایج: 70481  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
G St John N Brot J Ruan H Erdjument-Bromage P Tempst H Weissbach C Nathan

Inducible nitric oxide synthase (iNOS) plays an important role in host defense. Macrophages expressing iNOS release the reactive nitrogen intermediates (RNI) nitrite and S-nitrosoglutathione (GSNO), which are bactericidal in vitro at a pH characteristic of the phagosome of activated macrophages. We sought to characterize the active intrabacterial forms of these RNI and their molecular targets. ...

Journal: :Molecular & cellular proteomics : MCP 2011
Bart Ghesquière Veronique Jonckheere Niklaas Colaert Joost Van Durme Evy Timmerman Marc Goethals Joost Schymkowitz Frederic Rousseau Joël Vandekerckhove Kris Gevaert

We here present a new method to measure the degree of protein-bound methionine sulfoxide formation at a proteome-wide scale. In human Jurkat cells that were stressed with hydrogen peroxide, over 2000 oxidation-sensitive methionines in more than 1600 different proteins were mapped and their extent of oxidation was quantified. Meta-analysis of the sequences surrounding the oxidized methionine res...

Journal: :Infection and immunity 1982
M F Tsan

The myeloperoxidase (MPO)-mediated decarboxylation of amino acids and the MPO-mediated oxidation of methionine, two potential bactericidal mechanisms, were compared. In the presence of the MPO system (MPO, 50 mU/ml; H(2)O(2), 0.1 mM; Cl(-), 75 mM), 50% of alanine (0.1 mM) was decarboxylated, whereas only 5% of methionine (0.1 mM) was decarboxylated. In contrast, under similar conditions, 80% of...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1983
H Fliss H Weissbach N Brot

A simple assay for the detection of 35S-labeled methionine sulfoxide residues in proteins is described. The assay, which is based on the ability of CNBr to react with methionine but not with methionine sulfoxide, requires the prelabeling of cellular proteins with [35S]methionine. The assay was used to study the extent of methionine oxidation in newly synthesized proteins of both activated and q...

Journal: :Journal of Biological Chemistry 1997

Journal: :The Journal of biological chemistry 2006
Daphna Sagher David Brunell Nathan Brot Bert L Vallee Herbert Weissbach

In a recent study on the reducing requirement for the methionine sulfoxide reductases (Msr) (Sagher, D., Brunell, D., Hejtmancik, J. F., Kantorow, M., Brot, N. & Weissbach, H. (2006) Proc. Natl. Acad. Sci. U. S. A. 103, 8656-8661), we have shown that thioredoxin, although an excellent reducing system for Escherichia coli MsrA and MsrB and bovine MsrA, is not an efficient reducing agent for eith...

Journal: :Journal of bacteriology 2000
T R Kannan J B Baseman

We used Bacillus subtilis to express UGA-containing Mycoplasma genes encoding the P30 adhesin (one UGA) of Mycoplasma pneumoniae and methionine sulfoxide reductase (two UGAs) of Mycoplasma genitalium. Due to natural UGA suppression, these Mycoplasma genes were expressed as full-length protein products, but at relatively low efficiency, in recombinant wild-type Bacillus. The B. subtilis-expresse...

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