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