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-Structure paper
Title | Aryl tetrahydropyridine inhibitors of farnesyltransferase: bioavailable analogues with improved cellular potency. |
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Journal, issue, pages | Bioorg. Med. Chem. Lett., Vol. 13, Page 1363-1366, Year 2003 |
Publish date | Nov 22, 2002 (structure data deposition date) |
![]() | Gwaltney II, S.L. / O'Connor, S.J. / Nelson, L.T. / Sullivan, G.M. / Imade, H. / Wang, W. / Hasvold, L. / Li, Q. / Cohen, J. / Gu, W.Z. ...Gwaltney II, S.L. / O'Connor, S.J. / Nelson, L.T. / Sullivan, G.M. / Imade, H. / Wang, W. / Hasvold, L. / Li, Q. / Cohen, J. / Gu, W.Z. / Tahir, S.K. / Bauch, J. / Marsh, K. / Ng, S.C. / Frost, D.J. / Zhang, H. / Muchmore, S. / Jakob, C.G. / Stoll, V. / Hutchins, C. / Rosenberg, S.H. / Sham, H.L. |
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Methods | X-ray diffraction |
Resolution | 3.2 Å |
Structure data | ![]() PDB-1n9a: |
Chemicals | ![]() ChemComp-ZN: ![]() ChemComp-HFP: ![]() ChemComp-FTI: |
Source |
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![]() | TRANSFERASE / Farnesyltransferase / tetrahydropyridine / Prenyltransferase |