Tsivkovskii, Ruslan <br/><br/>
The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B.  [electronic resource] 

 -  The Journal of biological chemistry  Apr 2003 
 - 13302-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0021-9258 
<br/><br/><label>Standard No.: </label>10.1074/jbc.M300034200  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--chemistry<br/>Adenosine Triphosphate--metabolism<br/>Amino Acid Sequence<br/>Amino Acid Substitution<br/>Base Sequence<br/>Binding Sites<br/>Cation Transport Proteins--chemistry<br/>Cell Membrane--ultrastructure<br/>Copper-Transporting ATPases<br/>DNA Primers<br/>Hepatolenticular Degeneration--enzymology<br/>Histidine<br/>Humans<br/>Models, Molecular<br/>Molecular Sequence Data<br/>Mutagenesis, Site-Directed<br/>Protein Folding<br/>Protein Structure, Secondary<br/>Recombinant Proteins--chemistry<br/>Sequence Alignment<br/>Sequence Homology, Amino Acid