This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
3fz1
From Proteopedia
Crystal structure of a benzthiophene inhibitor bound to human Cyclin-dependent Kinase-2 (CDK-2)
Template:ABSTRACT PUBMED 19616942
About this Structure
3FZ1 is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Anderson DR, Meyers MJ, Kurumbail RG, Caspers N, Poda GI, Long SA, Pierce BS, Mahoney MW, Mourey RJ, Parikh MD. Benzothiophene inhibitors of MK2. Part 2: improvements in kinase selectivity and cell potency. Bioorg Med Chem Lett. 2009 Aug 15;19(16):4882-4. Epub 2009 Feb 8. PMID:19616942 doi:10.1016/j.bmcl.2009.02.017
Page seeded by OCA on Mon Sep 21 20:15:54 2009
Categories: Cyclin-dependent kinase | Homo sapiens | Caspers, N. | Kurumbail, R G. | Atp-binding | Benzothiophene | Cdk-2 | Cell cycle | Cell division | Cell divison kinase-2 | Cyclin | Kinase | Mapkap kinase-2 | Mitosis | Mk-2 | Mk2 | Nucleotide-binding | Phosphoprotein | Polymorphism | Ser/thr kinase | Serine/threonine-protein kinase | Transferase
