000 | 01781 a2200469 4500 | ||
---|---|---|---|
005 | 20250514055558.0 | ||
264 | 0 | _c20030703 | |
008 | 200307s 0 0 eng d | ||
022 | _a0021-9258 | ||
024 | 7 |
_a10.1074/jbc.M300034200 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aTsivkovskii, Ruslan | |
245 | 0 | 0 |
_aThe role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B. _h[electronic resource] |
260 |
_bThe Journal of biological chemistry _cApr 2003 |
||
300 |
_a13302-8 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. | ||
650 | 0 | 4 |
_aAdenosine Triphosphatases _xchemistry |
650 | 0 | 4 |
_aAdenosine Triphosphate _xmetabolism |
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aAmino Acid Substitution |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aBinding Sites |
650 | 0 | 4 |
_aCation Transport Proteins _xchemistry |
650 | 0 | 4 |
_aCell Membrane _xultrastructure |
650 | 0 | 4 | _aCopper-Transporting ATPases |
650 | 0 | 4 | _aDNA Primers |
650 | 0 | 4 |
_aHepatolenticular Degeneration _xenzymology |
650 | 0 | 4 | _aHistidine |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aModels, Molecular |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutagenesis, Site-Directed |
650 | 0 | 4 | _aProtein Folding |
650 | 0 | 4 | _aProtein Structure, Secondary |
650 | 0 | 4 |
_aRecombinant Proteins _xchemistry |
650 | 0 | 4 | _aSequence Alignment |
650 | 0 | 4 | _aSequence Homology, Amino Acid |
700 | 1 | _aEfremov, Roman G | |
700 | 1 | _aLutsenko, Svetlana | |
773 | 0 |
_tThe Journal of biological chemistry _gvol. 278 _gno. 15 _gp. 13302-8 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1074/jbc.M300034200 _zAvailable from publisher's website |
999 |
_c12351429 _d12351429 |