The transmembrane domains of the human multidrug resistance P-glycoprotein are sufficient to mediate drug binding and trafficking to the cell surface. [electronic resource]
- The Journal of biological chemistry Aug 1999
- 24759-65 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0021-9258
10.1074/jbc.274.35.24759 doi
ATP Binding Cassette Transporter, Subfamily B, Member 1--chemistry Binding Sites Capsaicin--pharmacology Cell Line Cyclosporine--pharmacology Gene Expression Regulation--drug effects Glycosylation Hexosaminidases--metabolism Humans Mannosyl-Glycoprotein Endo-beta-N-Acetylglucosaminidase--metabolism Membrane Proteins--metabolism Mutation Nucleotides--metabolism Peptide Fragments--metabolism Protein Binding Transfection Trypsin--metabolism Verapamil--pharmacology Vinblastine--pharmacology