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]
Producer: 20030703Description: 13302-8 p. digitalISSN:- 0021-9258
- Adenosine Triphosphatases -- chemistry
- Adenosine Triphosphate -- metabolism
- Amino Acid Sequence
- Amino Acid Substitution
- Base Sequence
- Binding Sites
- Cation Transport Proteins -- chemistry
- Cell Membrane -- ultrastructure
- Copper-Transporting ATPases
- DNA Primers
- Hepatolenticular Degeneration -- enzymology
- Histidine
- Humans
- Models, Molecular
- Molecular Sequence Data
- Mutagenesis, Site-Directed
- Protein Folding
- Protein Structure, Secondary
- Recombinant Proteins -- chemistry
- Sequence Alignment
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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