3pe2
From Proteopedia
(Difference between revisions)
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- | + | [[Image:3pe2.jpg|left|200px]] | |
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3pe2", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
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+ | {{STRUCTURE_3pe2| PDB=3pe2 | SCENE= }} | ||
- | + | ===Crystal structure of human protein kinase CK2 in complex with the inhibitor CX-5011=== | |
- | Description: Crystal structure of human protein kinase CK2 in complex with the inhibitor CX-5011 | ||
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+ | The line below this paragraph, {{ABSTRACT_PUBMED_21870818}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 21870818 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_21870818}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | [[3pe2]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3PE2 OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:021870818</ref><ref group="xtra">PMID:019432557</ref><references group="xtra"/> | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Non-specific serine/threonine protein kinase]] | ||
+ | [[Category: Battistutta, R.]] | ||
+ | [[Category: Haddach, M.]] | ||
+ | [[Category: Lolli, G.]] | ||
+ | [[Category: Papinutto, E.]] | ||
+ | [[Category: Pierre, F.]] | ||
+ | [[Category: Ryckman, D M.]] | ||
+ | [[Category: Ck2-inhibitor complex]] | ||
+ | [[Category: Kinase]] | ||
+ | [[Category: Transferase]] | ||
+ | [[Category: Transferase-transferase inhibitor complex]] |
Revision as of 06:10, 7 September 2011
Crystal structure of human protein kinase CK2 in complex with the inhibitor CX-5011
Template:ABSTRACT PUBMED 21870818
About this Structure
3pe2 is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Battistutta R, Cozza G, Pierre F, Papinutto E, Lolli G, Sarno S, O'Brien SE, Siddiqui-Jain A, Haddach M, Anderes K, Ryckman DM, Meggio F, Pinna LA. Unprecedented selectivity and structural determinants of a new class of protein kinase CK2 inhibitors in clinical stage for the treatment of cancer. Biochemistry. 2011 Aug 26. PMID:21870818 doi:10.1021/bi2008382
- Cozza G, Mazzorana M, Papinutto E, Bain J, Elliott M, di Maira G, Gianoncelli A, Pagano MA, Sarno S, Ruzzene M, Battistutta R, Meggio F, Moro S, Zagotto G, Pinna LA. Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2. Biochem J. 2009 Jul 15;421(3):387-95. PMID:19432557 doi:10.1042/BJ20090069