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-Structure paper
Title | The crystal structure of human protein farnesyltransferase reveals the basis for inhibition by CaaX tetrapeptides and their mimetics. |
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Journal, issue, pages | Proc. Natl. Acad. Sci. USA, Vol. 98, Page 12948-12953, Year 2001 |
Publish date | Jun 11, 2001 (structure data deposition date) |
![]() | Long, S.B. / Hancock, P.J. / Kral, A.M. / Hellinga, H.W. / Beese, L.S. |
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Methods | X-ray diffraction |
Resolution | 2 - 2.3 Å |
Structure data | ![]() PDB-1jcq: ![]() PDB-1jcr: ![]() PDB-1jcs: |
Chemicals | ![]() ChemComp-ACY: ![]() ChemComp-ZN: ![]() ChemComp-FPP: ![]() ChemComp-739: ![]() ChemComp-HOH: ![]() ChemComp-FII: |
Source |
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![]() | TRANSFERASE / FTASE / PFT / PFTASE / FT / FPT / FARNESYLTRANSFERASE / FARNESYL TRANSFERASE / FARNESYL PROTEIN TRANSFERASE / CAAX / RAS / CANCER / TUMOR REGRESSION / L-739 / 750 / PEPTIDOMIMETIC / INHIBITOR / TRANSFERASE/TRANSFERASE INHIBITOR / TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX |