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.
3d4q
From Proteopedia
Pyrazole-based inhibitors of B-Raf kinase
Template:ABSTRACT PUBMED 18676143
About this Structure
3D4Q is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Hansen JD, Grina J, Newhouse B, Welch M, Topalov G, Littman N, Callejo M, Gloor S, Martinson M, Laird E, Brandhuber BJ, Vigers G, Morales T, Woessner R, Randolph N, Lyssikatos J, Olivero A. Potent and selective pyrazole-based inhibitors of B-Raf kinase. Bioorg Med Chem Lett. 2008 Aug 15;18(16):4692-5. Epub 2008 Jul 5. PMID:18676143 doi:10.1016/j.bmcl.2008.07.002
Page seeded by OCA on Tue Feb 17 08:57:48 2009
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Brandhuber, B J | Morales, T. | Vigers, G P.A | Atp-binding | Cardiomyopathy | Cytoplasm | Disease mutation | Kinase | Metal-binding | Nucleotide-binding | Phorbol-ester binding | Phosphoprotein | Polymorphism | Proto-oncogene | Serine/threonine-protein kinase | Transferase | Zinc | Zinc-finger
