We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.
3ezv
From Proteopedia
Contents |
CDK-2 with indazole inhibitor 9 bound at its active site
Template:ABSTRACT PUBMED 19097791
About this Structure
3ezv is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Trujillo JI, Kiefer JR, Huang W, Thorarensen A, Xing L, Caspers NL, Day JE, Mathis KJ, Kretzmer KK, Reitz BA, Weinberg RA, Stegeman RA, Wrightstone A, Christine L, Compton R, Li X. 2-(6-Phenyl-1H-indazol-3-yl)-1H-benzo[d]imidazoles: design and synthesis of a potent and isoform selective PKC-zeta inhibitor. Bioorg Med Chem Lett. 2009 Feb 1;19(3):908-11. Epub 2008 Dec 6. PMID:19097791 doi:10.1016/j.bmcl.2008.11.105
Categories: Cyclin-dependent kinase | Homo sapiens | Caspers, N L. | Christine, L. | Compton, R. | Day, J E. | Huang, W. | Kiefer, J R. | Kretzmer, K K. | Li, X. | Mathis, K J. | Reitz, B A. | Stegeman, R A. | Thorarensen, A. | Trujillo, J I. | Weinberg, R A. | Wrightstone, A. | Xing, L. | Atp-binding | Cell cycle | Cell division | Inhibitor | Kinase | Mitosis | Nucleotide-binding | Phosphoprotein | Pkc | Protein kinase | Serine/threonine-protein kinase | Transferase
