ABCB1 p.Gly432Ser

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PMID: 7665554 [PubMed] Loo TW et al: "Rapid purification of human P-glycoprotein mutants expressed transiently in HEK 293 cells by nickel-chelate chromatography and characterization of their drug-stimulated ATPase activities."
No. Sentence Comment
95 To determine the contribution of either nucleotide-binding domain to drug-stimulatable ATPase activity, mutations were made to the core amino acids (G432S, K433M, G1075S, and K1076M, respectively) of the homology A consensus sequences.
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ABCB1 p.Gly432Ser 7665554:95:149
status: NEW
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122 E, wild type; q, Cys-less; f, mutant G432S.
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ABCB1 p.Gly432Ser 7665554:122:37
status: NEW
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PMID: 8549739 [PubMed] Senior AE et al: "The catalytic cycle of P-glycoprotein."
No. Sentence Comment
103 Loo and Clarke [37] extended this approach, showing that the mutations K433M, K1076M, G432S and G1075S in the Homology A sequences of either NBS1 or NBS2 in human Pgp abolish drug-exclusion capability in cells and eliminate ATPase activity in membranes.
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ABCB1 p.Gly432Ser 8549739:103:86
status: NEW
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