1r58: Difference between revisions

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[[Image:1r58.gif|left|200px]]
{{Seed}}
[[Image:1r58.png|left|200px]]


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{{STRUCTURE_1r58|  PDB=1r58  |  SCENE=  }}  
{{STRUCTURE_1r58|  PDB=1r58  |  SCENE=  }}  


'''Crystal Structure of MetAP2 complexed with A357300'''
===Crystal Structure of MetAP2 complexed with A357300===




==Overview==
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Substituted 3-amino-2-hydroxyamides and related hydroxyamides and acylhydrazines were identified as inhibitors of human methionine aminopeptidase-2 (MetAP2). Examination of substituents through parallel synthesis and iterative structure-based design allowed the identification of potent inhibitors with good selectivity against MetAP1. Diacylhydrazine 3t (A-357300) was identified as an analogue displaying inhibition of methionine processing and cellular proliferation in human microvascular endothelial cells (HMVEC).
The line below this paragraph, {{ABSTRACT_PUBMED_15012983}}, adds the Publication Abstract to the page
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{{ABSTRACT_PUBMED_15012983}}


==About this Structure==
==About this Structure==
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[[Category: Yang, F.]]
[[Category: Yang, F.]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]
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