2xiz
From Proteopedia
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[[Image:2xiz.png|left|200px]] | [[Image:2xiz.png|left|200px]] | ||
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{{STRUCTURE_2xiz| PDB=2xiz | SCENE= }} | {{STRUCTURE_2xiz| PDB=2xiz | SCENE= }} | ||
===PROTEIN KINASE PIM-1 IN COMPLEX WITH FRAGMENT-3 FROM CRYSTALLOGRAPHIC FRAGMENT SCREEN=== | ===PROTEIN KINASE PIM-1 IN COMPLEX WITH FRAGMENT-3 FROM CRYSTALLOGRAPHIC FRAGMENT SCREEN=== | ||
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{{ABSTRACT_PUBMED_21358046}} | {{ABSTRACT_PUBMED_21358046}} | ||
==About this Structure== | ==About this Structure== | ||
- | [[2xiz]] 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=2XIZ OCA]. | + | [[2xiz]] 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=2XIZ 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:021358046</ref><references group="xtra"/> |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Badock, V.]] | [[Category: Badock, V.]] | ||
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[[Category: Schafer, M.]] | [[Category: Schafer, M.]] | ||
[[Category: Schulz, M N.]] | [[Category: Schulz, M N.]] | ||
+ | [[Category: Phosphorylation]] | ||
+ | [[Category: Transferase]] |
Revision as of 18:33, 26 July 2012
Contents |
PROTEIN KINASE PIM-1 IN COMPLEX WITH FRAGMENT-3 FROM CRYSTALLOGRAPHIC FRAGMENT SCREEN
Template:ABSTRACT PUBMED 21358046
About this Structure
2xiz 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
- Schulz MN, Fanghanel J, Schafer M, Badock V, Briem H, Boemer U, Nguyen D, Husemann M, Hillig RC. A crystallographic fragment screen identifies cinnamic acid derivatives as starting points for potent Pim-1 inhibitors. Acta Crystallogr D Biol Crystallogr. 2011 Mar;67(Pt 3):156-66. Epub 2011, Feb 15. PMID:21358046 doi:10.1107/S0907444910054144