Loo, T W <br/><br/>
Covalent modification of human P-glycoprotein mutants containing a single cysteine in either nucleotide-binding fold abolishes drug-stimulated ATPase activity.  [electronic resource] 

 -  The Journal of biological chemistry  Sep 1995 
 - 22957-61 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-9258 
<br/><br/><label>Standard No.: </label>10.1074/jbc.270.39.22957  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATP Binding Cassette Transporter, Subfamily B, Member 1--biosynthesis<br/>Adenosine Triphosphatases--biosynthesis<br/>Amino Acid Sequence<br/>Animals<br/>Binding Sites<br/>Calcium Channel Blockers--pharmacology<br/>Cell Line<br/>Cell Membrane--metabolism<br/>Consensus Sequence<br/>Cysteine<br/>Enzyme Inhibitors--pharmacology<br/>Ethylmaleimide--pharmacology<br/>Humans<br/>Kinetics<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Nucleotides--metabolism<br/>Protein Folding<br/>Recombinant Proteins--biosynthesis<br/>Sequence Deletion<br/>Spodoptera<br/>Transfection<br/>Verapamil--pharmacology