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6. The drug-binding pocket of the human multidrug resistance P-glycoprotein is accessible to the aqueous medium. Loo TW, Bartlett MC, Clarke DM. Biochemistry; 2004 Sep 28; 43(38):12081-9. PubMed ID: 15379547 [Abstract] [Full Text] [Related]
7. Structural flexibility of the linker region of human P-glycoprotein permits ATP hydrolysis and drug transport. Hrycyna CA, Airan LE, Germann UA, Ambudkar SV, Pastan I, Gottesman MM. Biochemistry; 1998 Sep 29; 37(39):13660-73. PubMed ID: 9753453 [Abstract] [Full Text] [Related]
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