2uw3
From Proteopedia
Line 1: | Line 1: | ||
[[Image:2uw3.jpg|left|200px]] | [[Image:2uw3.jpg|left|200px]] | ||
- | + | <!-- | |
- | + | The line below this paragraph, containing "STRUCTURE_2uw3", creates the "Structure Box" on the page. | |
- | + | You may change the PDB parameter (which sets the PDB file loaded into the applet) | |
- | + | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | |
- | + | or leave the SCENE parameter empty for the default display. | |
- | | | + | --> |
- | | | + | {{STRUCTURE_2uw3| PDB=2uw3 | SCENE= }} |
- | + | ||
- | + | ||
- | }} | + | |
'''STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE''' | '''STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE''' | ||
+ | |||
+ | ==Overview== | ||
+ | Using fragment-based screening techniques, 5-methyl-4-phenyl-1H-pyrazole (IC50 80 microM) was identified as a novel, low molecular weight inhibitor of protein kinase B (PKB). Herein we describe the rapid elaboration of highly potent and ligand efficient analogues using a fragment growing approach. Iterative structure-based design was supported by protein-ligand structure determinations using a PKA-PKB "chimera" and a final protein-ligand structure of a lead compound in PKBbeta itself. | ||
==About this Structure== | ==About this Structure== | ||
2UW3 is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2UW3 OCA]. | 2UW3 is a [[Protein complex]] structure of sequences from [http://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2UW3 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | Identification of inhibitors of protein kinase B using fragment-based lead discovery., Saxty G, Woodhead SJ, Berdini V, Davies TG, Verdonk ML, Wyatt PG, Boyle RG, Barford D, Downham R, Garrett MD, Carr RA, J Med Chem. 2007 May 17;50(10):2293-6. Epub 2007 Apr 24. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/17451234 17451234] | ||
[[Category: Bos taurus]] | [[Category: Bos taurus]] | ||
[[Category: Protein complex]] | [[Category: Protein complex]] | ||
- | [[Category: | + | [[Category: CAMP-dependent protein kinase]] |
[[Category: Barford, D.]] | [[Category: Barford, D.]] | ||
[[Category: Berdini, V.]] | [[Category: Berdini, V.]] | ||
Line 31: | Line 34: | ||
[[Category: Woodhead, S J.]] | [[Category: Woodhead, S J.]] | ||
[[Category: Wyatt, P G.]] | [[Category: Wyatt, P G.]] | ||
- | [[Category: | + | [[Category: Atp-binding]] |
- | [[Category: | + | [[Category: Camp]] |
- | [[Category: | + | [[Category: Kinase]] |
- | [[Category: | + | [[Category: Lipoprotein]] |
- | [[Category: | + | [[Category: Myristate]] |
- | [[Category: | + | [[Category: Nuclear protein]] |
- | [[Category: | + | [[Category: Nucleotide-binding]] |
- | [[Category: | + | [[Category: Phosphorylation]] |
- | [[Category: | + | [[Category: Protein kinase inhibitor]] |
- | [[Category: | + | [[Category: Serine/threonine-protein kinase]] |
- | [[Category: | + | [[Category: Transferase]] |
- | [[Category: | + | [[Category: Transferase/inhibitor complex]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 30 13:32:13 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 10:32, 30 April 2008
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE
Overview
Using fragment-based screening techniques, 5-methyl-4-phenyl-1H-pyrazole (IC50 80 microM) was identified as a novel, low molecular weight inhibitor of protein kinase B (PKB). Herein we describe the rapid elaboration of highly potent and ligand efficient analogues using a fragment growing approach. Iterative structure-based design was supported by protein-ligand structure determinations using a PKA-PKB "chimera" and a final protein-ligand structure of a lead compound in PKBbeta itself.
About this Structure
2UW3 is a Protein complex structure of sequences from Bos taurus. Full crystallographic information is available from OCA.
Reference
Identification of inhibitors of protein kinase B using fragment-based lead discovery., Saxty G, Woodhead SJ, Berdini V, Davies TG, Verdonk ML, Wyatt PG, Boyle RG, Barford D, Downham R, Garrett MD, Carr RA, J Med Chem. 2007 May 17;50(10):2293-6. Epub 2007 Apr 24. PMID:17451234 Page seeded by OCA on Wed Apr 30 13:32:13 2008
Categories: Bos taurus | Protein complex | CAMP-dependent protein kinase | Barford, D. | Berdini, V. | Boyle, R G. | Carr, R A. | Davies, T G. | Downham, R. | Garrett, M D. | Saxty, G. | Verdonk, M L. | Woodhead, S J. | Wyatt, P G. | Atp-binding | Camp | Kinase | Lipoprotein | Myristate | Nuclear protein | Nucleotide-binding | Phosphorylation | Protein kinase inhibitor | Serine/threonine-protein kinase | Transferase | Transferase/inhibitor complex