3odk
From Proteopedia
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Revision as of 08:11, 3 November 2010
Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution
Template:ABSTRACT PUBMED 20932746
About this Structure
3ODK is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Potter A, Oldfield V, Nunns C, Fromont C, Ray S, Northfield CJ, Bryant CJ, Scrace SF, Robinson D, Matossova N, Baker L, Dokurno P, Surgenor AE, Davis B, Richardson CM, Murray JB, Moore JD. Discovery of cell-active phenyl-imidazole Pin1 inhibitors by structure-guided fragment evolution. Bioorg Med Chem Lett. 2010 Nov 15;20(22):6483-8. Epub 2010 Sep 17. PMID:20932746 doi:10.1016/j.bmcl.2010.09.063
Page seeded by OCA on Wed Nov 3 11:22:08 2010
Categories: Homo sapiens | Peptidylprolyl isomerase | Baker, L. | Bryant, C J. | Davis, B E. | Dokurno, P. | Fromont, C. | Matossova, N. | Moore, J D. | Murray, J B. | Northfield, C J. | Nunns, C. | Oldfield, V. | Potter, A. | Ray, S. | Richardson, C M. | Robinson, D. | Scrace, S F. | Surgenor, A E. | Cell cycle | Isomerase | Nucleus | Oncogenic transformation | Phosphoprotein | Ppiase | Proline directed kinase | Rotamase | Sbdd | Small molecule
