000 | 01486 a2200361 4500 | ||
---|---|---|---|
005 | 20250514014830.0 | ||
264 | 0 | _c20011207 | |
008 | 200112s 0 0 eng d | ||
022 | _a0027-8424 | ||
024 | 7 |
_a10.1073/pnas.241407898 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aLong, S B | |
245 | 0 | 0 |
_aThe crystal structure of human protein farnesyltransferase reveals the basis for inhibition by CaaX tetrapeptides and their mimetics. _h[electronic resource] |
260 |
_bProceedings of the National Academy of Sciences of the United States of America _cNov 2001 |
||
300 |
_a12948-53 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 |
_aAlkyl and Aryl Transferases _xantagonists & inhibitors |
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aCrystallography, X-Ray |
650 | 0 | 4 |
_aEnzyme Inhibitors _xpharmacology |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aModels, Molecular |
650 | 0 | 4 | _aMolecular Mimicry |
650 | 0 | 4 |
_aOligopeptides _xchemistry |
650 | 0 | 4 | _aProtein Conformation |
650 | 0 | 4 |
_aRecombinant Proteins _xantagonists & inhibitors |
700 | 1 | _aHancock, P J | |
700 | 1 | _aKral, A M | |
700 | 1 | _aHellinga, H W | |
700 | 1 | _aBeese, L S | |
773 | 0 |
_tProceedings of the National Academy of Sciences of the United States of America _gvol. 98 _gno. 23 _gp. 12948-53 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1073/pnas.241407898 _zAvailable from publisher's website |
999 |
_c11604368 _d11604368 |