Extracellularly Applied Br-TITU Inhibits the Na+/K+ Pump by Interacting with Tryptophan at the Entrance to the Cation Sites
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Veröffentlicht in: | Annals of the New York Academy of Sciences 2003-04, Vol.986 (1), p.287-289 |
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creator | YUDOWSKI, G. A. SHIMON, M. BAR GONZÁLEZ-LEBRERO, R. M. ROSSI, R. C. GARRAHAN, P. J. KARLISH, S. J. D. BEAUGÉ, L. |
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doi_str_mv | 10.1111/j.1749-6632.2003.tb07188.x |
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source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | Binding Sites Br-TITU cation-tryptophan interaction Cations - metabolism Enzyme Inhibitors - pharmacology Erythrocytes - enzymology Humans Isothiuronium - analogs & derivatives Isothiuronium - pharmacology Kinetics Na+/K+-ATPase entrance port Ouabain - pharmacology Sodium - blood Sodium-Potassium-Exchanging ATPase - antagonists & inhibitors Sodium-Potassium-Exchanging ATPase - blood Sodium-Potassium-Exchanging ATPase - chemistry Tryptophan tryptophan fluorescence |
title | Extracellularly Applied Br-TITU Inhibits the Na+/K+ Pump by Interacting with Tryptophan at the Entrance to the Cation Sites |
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