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23. ATP-binding properties of P glycoprotein from multidrug-resistant KB cells. Cornwell MM, Tsuruo T, Gottesman MM, Pastan I. FASEB J; 1987 Jul; 1(1):51-4. PubMed ID: 2886389 [Abstract] [Full Text] [Related]
24. The molecular interaction of the high affinity reversal agent XR9576 with P-glycoprotein. Martin C, Berridge G, Mistry P, Higgins C, Charlton P, Callaghan R. Br J Pharmacol; 1999 Sep; 128(2):403-11. PubMed ID: 10510451 [Abstract] [Full Text] [Related]
25. Proximity of bound Hoechst 33342 to the ATPase catalytic sites places the drug binding site of P-glycoprotein within the cytoplasmic membrane leaflet. Qu Q, Sharom FJ. Biochemistry; 2002 Apr 09; 41(14):4744-52. PubMed ID: 11926837 [Abstract] [Full Text] [Related]
26. The functional purification of P-glycoprotein is dependent on maintenance of a lipid-protein interface. Callaghan R, Berridge G, Ferry DR, Higgins CF. Biochim Biophys Acta; 1997 Sep 04; 1328(2):109-24. PubMed ID: 9315609 [Abstract] [Full Text] [Related]
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32. Combined mutation of catalytic glutamate residues in the two nucleotide binding domains of P-glycoprotein generates a conformation that binds ATP and ADP tightly. Tombline G, Bartholomew LA, Urbatsch IL, Senior AE. J Biol Chem; 2004 Jul 23; 279(30):31212-20. PubMed ID: 15159388 [Abstract] [Full Text] [Related]
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