2pvh

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[[Image:2pvh.png|left|200px]]
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{{STRUCTURE_2pvh| PDB=2pvh | SCENE= }}
{{STRUCTURE_2pvh| PDB=2pvh | SCENE= }}
===Structure-Based Design of Pyrazolo[1,5-a][1,3,5]triazine Derivatives as Potent Inhibitors of Protein Kinase CK2===
===Structure-Based Design of Pyrazolo[1,5-a][1,3,5]triazine Derivatives as Potent Inhibitors of Protein Kinase CK2===
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{{ABSTRACT_PUBMED_17540560}}
{{ABSTRACT_PUBMED_17540560}}
==About this Structure==
==About this Structure==
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2PVH is a 1 chain structure of sequence from [http://en.wikipedia.org/wiki/Zea_mays Zea mays]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2PVH OCA].
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[[2pvh]] is a 1 chain structure of [[Casein kinase]] with sequence from [http://en.wikipedia.org/wiki/Zea_mays Zea mays]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2PVH OCA].
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==See Also==
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*[[Casein kinase|Casein kinase]]
==Reference==
==Reference==
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<ref group="xtra">PMID:17540560</ref><references group="xtra"/>
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<ref group="xtra">PMID:017540560</ref><references group="xtra"/>
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Non-specific serine/threonine protein kinase]]
[[Category: Zea mays]]
[[Category: Zea mays]]
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[[Category: Structure-based drug design]]
[[Category: Structure-based drug design]]
[[Category: Transferase]]
[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 11:22:09 2009''
 

Revision as of 10:34, 25 July 2012

Template:STRUCTURE 2pvh

Contents

Structure-Based Design of Pyrazolo[1,5-a][1,3,5]triazine Derivatives as Potent Inhibitors of Protein Kinase CK2

Template:ABSTRACT PUBMED 17540560

About this Structure

2pvh is a 1 chain structure of Casein kinase with sequence from Zea mays. Full crystallographic information is available from OCA.

See Also

Reference

  • Nie Z, Perretta C, Erickson P, Margosiak S, Almassy R, Lu J, Averill A, Yager KM, Chu S. Structure-based design, synthesis, and study of pyrazolo[1,5-a][1,3,5]triazine derivatives as potent inhibitors of protein kinase CK2. Bioorg Med Chem Lett. 2007 Aug 1;17(15):4191-5. Epub 2007 May 18. PMID:17540560 doi:10.1016/j.bmcl.2007.05.041

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