3f5x
CDK-2-Cyclin complex with indazole inhibitor 9 bound at its active siteCDK-2-Cyclin complex with indazole inhibitor 9 bound at its active site
Template:ABSTRACT PUBMED 19097791
About this StructureAbout this Structure
3f5x is a 4 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ 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
Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCACategories:
- Pages with broken file links
- 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
- Cyclin
- Inhibitor
- Kinase
- Mitosis
- Nucleotide-binding
- Nucleus
- Phosphoprotein
- Pkc
- Protein kinase
- Serine/threonine-protein kinase
- Transferase
- Transferase-cell cycle complex