نتایج جستجو برای: ribonucleotide reductase

تعداد نتایج: 45665  

Journal: :Molecular cancer therapeutics 2005
Lars Petter Jordheim Olivier Guittet Michel Lepoivre Carlos M Galmarini Charles Dumontet

Resistance to cytotoxic nucleoside analogues is a major problem in cancer treatment. The cellular mechanisms involved in this phenomenon have been studied for several years, and some factors have been identified. However, this resistance seems to be multifactorial and more studies are needed to gain better insight into this domain. For this purpose, we developed a gemcitabine-resistant cell lin...

Journal: :Blood 1997
H Iwasaki P Huang M J Keating W Plunkett

The major actions of nucleoside analogs such as arabinosylcytosine (ara-C) and fludarabine occurs after their incorporation into DNA, during either replication or repair synthesis. The metabolic salvage and DNA incorporation of the normal nucleoside, deoxycytidine, is functionally compartmentalized toward repair synthesis in a process regulated by ribonucleotide reductase. The aim of this study...

Journal: :Journal of Biological Chemistry 1972

Journal: :Genes 2023

Vitamin B12 is an enzymatic cofactor that essential for both eukaryotes and prokaryotes. The development of life in extreme environments depends on cofactors such as vitamin well. genomes twelve microorganisms isolated from the deep subsurface Iberian Pyrite Belt have been analyzed search activities require or are involved its synthesis import. Results revealed needed by these several enzymes r...

Journal: :Journal of Biological Chemistry 1974

Journal: :The Journal of biological chemistry 1990
T Joelson B M Sjöberg H Eklund

The active site sequence of T4 thioredoxin, Cys-Val-Tyr-Cys, has been modified in two positions to Cys-Gly-Pro-Cys to mimic that of Escherichia coli thioredoxin. The two point mutants Cys-Gly-Tyr-Cys and Cys-Val-Pro-Cys have also been constructed. The mutant proteins have similar reaction rates with T4 ribonucleotide reductase as has the wild-type T4 thioredoxin. Mutant T4 thioredoxins with Pro...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1975
S Munavalli D V Parker F D Hamilton

Euglena gracilis contains a protein system which can utilize the reducing power of NADPH in the ribonucleotide reductase-catalyzed reduction of CTP. The proteins required for this reaction are a flavoprotien with a molecular weight of approximately 185,000 which is functionally similar to thioredoxin reductase (NADPH), EC 1.6.4.5, and another protein (Protein I) whose function in the reaction i...

Journal: :Cancer research 1979
J G Cory A E Fleischer

It had been shown previously that the ribonucleotide reductase from mouse tumor consisted of two nonidentical components (Tris and dye fractions, each prepared from the 20 to 40% (NH/)2SO4 protein fraction containing the ribonucleotide reductase activity by blue dextran-Sepharose chromatography). The individual components either separated or present in the intact enzyme can be specifically and ...

2002
LARS THELANDER

Ribonucleoside diphosphate reductase consists of two nonidentical subunits, proteins Bl and B2. The enzyme catalyzes the reduction of ribonucleotides to the corresponding deoxyribonucleotides. The electrons required in this reduction are transported from NADPH via a flavoprotein, thioredoxin reductase, to a low molecular weight protein, thioredoxin. The reduced form of thioredoxin acts as hydro...

2001
Mikaela Luthman Arne Holmgren

The protein glutaredoxin, required for GSH-dependent ribonucleotide reduction, has been purified to homogeneity from calf thymus. The preparative method consisted of ammonium sulfate precipitation and three chromatography steps on DEAEkellulose, Sephadex G-50, and CM-Sepharose. Calf thymus glutaredoxin was assayed on the basis of its inherent GSH-disulfide transhydrogenase activity. Glutaredoxi...

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