1m2p

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[[Image:1m2p.jpg|left|200px]]
[[Image:1m2p.jpg|left|200px]]
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{{Structure
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<!--
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|PDB= 1m2p |SIZE=350|CAPTION= <scene name='initialview01'>1m2p</scene>, resolution 2.00&Aring;
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The line below this paragraph, containing "STRUCTURE_1m2p", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=HNA:1,8-DI-HYDROXY-4-NITRO-ANTHRAQUINONE'>HNA</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Non-specific_serine/threonine_protein_kinase Non-specific serine/threonine protein kinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.7.11.1 2.7.11.1] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1m2p| PDB=1m2p | SCENE= }}
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|RELATEDENTRY=[[1j91|1J91]], [[1jam|1JAM]], [[1f0q|1F0Q]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1m2p FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1m2p OCA], [http://www.ebi.ac.uk/pdbsum/1m2p PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1m2p RCSB]</span>
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}}
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'''Crystal structure of 1,8-di-hydroxy-4-nitro-anthraquinone/CK2 kinase complex'''
'''Crystal structure of 1,8-di-hydroxy-4-nitro-anthraquinone/CK2 kinase complex'''
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[[Category: Zagotto, G.]]
[[Category: Zagotto, G.]]
[[Category: Zanotti, G.]]
[[Category: Zanotti, G.]]
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[[Category: inhibitor-enzyme complex]]
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[[Category: Inhibitor-enzyme complex]]
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[[Category: kinase]]
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[[Category: Kinase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 00:33:41 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:10:31 2008''
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Revision as of 21:33, 2 May 2008

Template:STRUCTURE 1m2p

Crystal structure of 1,8-di-hydroxy-4-nitro-anthraquinone/CK2 kinase complex


Overview

Protein kinases play key roles in signal transduction and therefore are among the most attractive targets for drug design. The pharmacological aptitude of protein kinase inhibitors is highlighted by the observation that various diseases with special reference to cancer are because of the abnormal expression/activity of individual kinases. The resolution of the three-dimensional structure of the target kinase in complex with inhibitors is often the starting point for the rational design of this kind of drugs, some of which are already in advanced clinical trial or even in clinical practice. Here we present and discuss three new crystal structures of ATP site-directed inhibitors in complex with "casein kinase-2" (CK2), a constitutively active protein kinase implicated in a variety of cellular functions and misfunctions. With the help of theoretical calculations, we disclose some key features underlying the inhibitory efficiency of anthraquinone derivatives, outlining three different binding modes into the active site. In particular, we show that a nitro group in a hydroxyanthraquinone scaffold decreases the inhibitory constants K(i) because of electron-withdrawing and resonance effects that enhance the polarization of hydroxylic substituents in paraposition.

About this Structure

1M2P is a Single protein structure of sequence from Zea mays. Full crystallographic information is available from OCA.

Reference

Inhibition of protein kinase CK2 by anthraquinone-related compounds. A structural insight., De Moliner E, Moro S, Sarno S, Zagotto G, Zanotti G, Pinna LA, Battistutta R, J Biol Chem. 2003 Jan 17;278(3):1831-6. Epub 2002 Nov 4. PMID:12419810 Page seeded by OCA on Sat May 3 00:33:41 2008

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