2xnb: Difference between revisions
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[[Image:2xnb.png|left|200px]] | [[Image:2xnb.png|left|200px]] | ||
{{STRUCTURE_2xnb| PDB=2xnb | SCENE= }} | {{STRUCTURE_2xnb| PDB=2xnb | SCENE= }} | ||
===Discovery and Characterisation of 2-Anilino-4-(thiazol-5-yl) pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents=== | ===Discovery and Characterisation of 2-Anilino-4-(thiazol-5-yl) pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents=== | ||
{{ABSTRACT_PUBMED_21035734}} | {{ABSTRACT_PUBMED_21035734}} | ||
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==See Also== | ==See Also== | ||
*[[Cell Division Protein Kinase 2]] | *[[Cell Division Protein Kinase 2|Cell Division Protein Kinase 2]] | ||
==Reference== | ==Reference== | ||
Revision as of 05:06, 26 July 2012
Discovery and Characterisation of 2-Anilino-4-(thiazol-5-yl) pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents
Template:ABSTRACT PUBMED 21035734
About this Structure
2xnb is a 1 chain structure of Cell Division Protein Kinase 2 with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Wang S, Griffiths G, Midgley CA, Barnett AL, Cooper M, Grabarek J, Ingram L, Jackson W, Kontopidis G, McClue SJ, McInnes C, McLachlan J, Meades C, Mezna M, Stuart I, Thomas MP, Zheleva DI, Lane DP, Jackson RC, Glover DM, Blake DG, Fischer PM. Discovery and characterization of 2-anilino-4- (thiazol-5-yl)pyrimidine transcriptional CDK inhibitors as anticancer agents. Chem Biol. 2010 Oct 29;17(10):1111-21. PMID:21035734 doi:10.1016/j.chembiol.2010.07.016
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Categories:
- Pages with broken file links
- Cyclin-dependent kinase
- Homo sapiens
- Barnett, A L.
- Blake, D G.
- Cooper, M.
- Fischer, P M.
- Glover, D M.
- Grabarek, J.
- Griffiths, G.
- Ingram, L.
- Jackson, R C.
- Jackson, W.
- Kontopidis, G.
- Lane, D P.
- Mcclue, S J.
- Mcinnes, C.
- Mclachlan, J.
- Meades, C.
- Mezna, M.
- Midgley, C A.
- Stuart, I.
- Thomas, M P.
- Wang, S.
- Zheleva, D I.
- Cdk9 inhibitor
- Cell cycle
- Transferase