000 | 01957 a2200553 4500 | ||
---|---|---|---|
005 | 20250513100516.0 | ||
264 | 0 | _c19961209 | |
008 | 199612s 0 0 eng d | ||
022 | _a0969-2126 | ||
024 | 7 |
_a10.1016/s0969-2126(96)00098-6 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBreton, R | |
245 | 0 | 0 |
_aThe structure of a complex of human 17beta-hydroxysteroid dehydrogenase with estradiol and NADP+ identifies two principal targets for the design of inhibitors. _h[electronic resource] |
260 |
_bStructure (London, England : 1993) _cAug 1996 |
||
300 |
_a905-15 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 |
_aAntineoplastic Agents _xchemistry |
650 | 0 | 4 |
_aBinding Sites _xdrug effects |
650 | 0 | 4 | _aCatalysis |
650 | 0 | 4 | _aCrystallography, X-Ray |
650 | 0 | 4 | _aDrug Design |
650 | 0 | 4 |
_aEnzyme Inhibitors _xchemistry |
650 | 0 | 4 |
_aEstradiol _xchemistry |
650 | 0 | 4 |
_aEstradiol Dehydrogenases _xantagonists & inhibitors |
650 | 0 | 4 |
_aEstrone _xmetabolism |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMacromolecular Substances |
650 | 0 | 4 | _aModels, Molecular |
650 | 0 | 4 | _aMolecular Conformation |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aNADP _xchemistry |
650 | 0 | 4 | _aOxidation-Reduction |
650 | 0 | 4 |
_aOxygen _xchemistry |
650 | 0 | 4 |
_aPlacenta _xenzymology |
650 | 0 | 4 |
_aProtein Binding _xdrug effects |
650 | 0 | 4 | _aProtein Conformation |
650 | 0 | 4 |
_aRecombinant Proteins _xchemistry |
650 | 0 | 4 |
_aSerine _xchemistry |
650 | 0 | 4 | _aSubstrate Specificity |
650 | 0 | 4 | _aTemperature |
650 | 0 | 4 |
_aTyrosine _xchemistry |
700 | 1 | _aHousset, D | |
700 | 1 | _aMazza, C | |
700 | 1 | _aFontecilla-Camps, J C | |
773 | 0 |
_tStructure (London, England : 1993) _gvol. 4 _gno. 8 _gp. 905-15 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0969-2126(96)00098-6 _zAvailable from publisher's website |
999 |
_c8800288 _d8800288 |