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2xm8
From Proteopedia
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[[Image:2xm8.png|left|200px]] | [[Image:2xm8.png|left|200px]] | ||
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{{STRUCTURE_2xm8| PDB=2xm8 | SCENE= }} | {{STRUCTURE_2xm8| PDB=2xm8 | SCENE= }} | ||
===CO-CRYSTAL STRUCTURE OF A SMALL MOLECULE INHIBITOR BOUND TO THE KINASE DOMAIN OF CHK2=== | ===CO-CRYSTAL STRUCTURE OF A SMALL MOLECULE INHIBITOR BOUND TO THE KINASE DOMAIN OF CHK2=== | ||
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{{ABSTRACT_PUBMED_21186793}} | {{ABSTRACT_PUBMED_21186793}} | ||
==About this Structure== | ==About this Structure== | ||
| - | [[2xm8]] 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=2XM8 OCA]. | + | [[2xm8]] is a 1 chain structure of [[Serine/threonine protein kinase]] 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=2XM8 OCA]. |
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| + | ==See Also== | ||
| + | *[[Serine/threonine protein kinase|Serine/threonine protein kinase]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:021186793</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Non-specific serine/threonine protein kinase]] | [[Category: Non-specific serine/threonine protein kinase]] | ||
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[[Category: Urban, F.]] | [[Category: Urban, F.]] | ||
[[Category: Welsh, E J.]] | [[Category: Welsh, E J.]] | ||
| + | [[Category: Cancer]] | ||
| + | [[Category: Transferase]] | ||
Revision as of 02:21, 27 July 2012
Contents |
CO-CRYSTAL STRUCTURE OF A SMALL MOLECULE INHIBITOR BOUND TO THE KINASE DOMAIN OF CHK2
Template:ABSTRACT PUBMED 21186793
About this Structure
2xm8 is a 1 chain structure of Serine/threonine protein kinase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Caldwell JJ, Welsh EJ, Matijssen C, Anderson VE, Antoni L, Boxall K, Urban F, Hayes A, Raynaud FI, Rigoreau LJ, Raynham T, Aherne GW, Pearl LH, Oliver AW, Garrett MD, Collins I. Structure-Based Design of Potent and Selective 2-(Quinazolin-2-yl)phenol Inhibitors of Checkpoint Kinase 2. J Med Chem. 2010 Dec 27. PMID:21186793 doi:10.1021/jm101150b
Categories: Homo sapiens | Non-specific serine/threonine protein kinase | Aherne, G W. | Anderson, V E. | Antoni, L. | Boxall, K. | Caldwell, J J. | Collins, I. | Garrett, M D. | Hayes, A. | Matijssen, C. | Oliver, A W. | Pearl, L H. | Raynaud, F I. | Raynham, T. | Rigoreau, L J. | Urban, F. | Welsh, E J. | Cancer | Transferase
