2o5k: Difference between revisions

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{{STRUCTURE_2o5k|  PDB=2o5k  |  SCENE=  }}  
{{STRUCTURE_2o5k|  PDB=2o5k  |  SCENE=  }}  


'''Crystal Structure of GSK3beta in complex with a benzoimidazol inhibitor'''
===Crystal Structure of GSK3beta in complex with a benzoimidazol inhibitor===




==Overview==
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A hydroxy functional group was introduced as the hydrogen bond donor and acceptor at the hinge region of protein kinase in order to develop novel ATP-competitive inhibitors. Several derivatives of 7-hydroxyl-1H-benzoimidazole were designed as inhibitors of glycogen synthase kinase-3beta with the help of ab initio calculations and a docking study. Enzymatic assay and an X-ray complex study showed that these designed compounds were highly potent ATP-competitive inhibitors.
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{{ABSTRACT_PUBMED_17764934}}


==About this Structure==
==About this Structure==
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[[Category: Gsk3beta]]
[[Category: Gsk3beta]]
[[Category: Transferase]]
[[Category: Transferase]]
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