1pxm | pdb_00001pxm
From Proteopedia
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 3-[4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamino]-phenol
About this Structure
1PXM is a 1 chain structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Wang S, Meades C, Wood G, Osnowski A, Anderson S, Yuill R, Thomas M, Mezna M, Jackson W, Midgley C, Griffiths G, Fleming I, Green S, McNae I, Wu SY, McInnes C, Zheleva D, Walkinshaw MD, Fischer PM. 2-Anilino-4-(thiazol-5-yl)pyrimidine CDK inhibitors: synthesis, SAR analysis, X-ray crystallography, and biological activity. J Med Chem. 2004 Mar 25;47(7):1662-75. PMID:15027857 doi:10.1021/jm0309957
Page seeded by OCA on Tue Feb 17 10:13:55 2009
Proteopedia Page Contributors and Editors (what is this?)
Categories:
- Pages with broken file links
- Homo sapiens
- Anderson, S.
- Fischer, P M.
- Griffiths, G.
- Jackson, W.
- McInnes, C.
- McNae, I.
- Meades, C.
- Midgley, C.
- Osnowski, A.
- Thomas, M.
- Walkinshaw, M D.
- Wang, S.
- Wood, G.
- Wu, S Y.
- Yuill, R.
- Zheleva, D.
- 3d-structure.
- Atp-binding
- Cell cycle
- Cell division
- Inhibition
- Mitosis
- Phosphorylation
- Protein kinase
- Serine/threonine-protein kinase
- Transferase
