2oaz

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{{STRUCTURE_2oaz| PDB=2oaz | SCENE= }}
{{STRUCTURE_2oaz| PDB=2oaz | SCENE= }}
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'''Human Methionine Aminopeptidase-2 Complexed with SB-587094'''
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===Human Methionine Aminopeptidase-2 Complexed with SB-587094===
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==Overview==
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High-throughput screening for inhibitors of the human metalloprotease, methionine aminopeptidase-2 (MetAP2), identified a potent class of 3-anilino-5-benzylthio-1,2,4-triazole compounds. Efficient array and interative synthesis of triazoles led to rapid SAR development around the aniline, benzylthio, and triazole moeities. Evaluation of these analogs in a human MetAP2 enzyme assay led to the identification of several inhibitors with potencies in the 50-100 picomolar range. The deleterious effects on inhibitor potency by methylation of the anilino-triazole nitrogens, as well as the X-ray crystal structure of triazole 102 bound in the active site of MetAP2, confirm the key interactions between the triazole nitrogens, the active site cobalt atoms, and the His-231 side-chain. The structure has also provided a rationale for interpreting SAR within the triazole series. Key aniline (2-isopropylphenyl) and sulfur substituents (furanylmethyl) identified in the SAR studies led to the identification of potent inhibitors (103 and 104) of endothelial cell proliferation. Triazoles 103 and 104 also exhibited dose-dependent activity in an aortic ring tissue model of angiogenesis highlighting the potential utility of MetAP2 inhibitors as anticancer agents.
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(as it appears on PubMed at http://www.pubmed.gov), where 17636946 is the PubMed ID number.
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{{ABSTRACT_PUBMED_17636946}}
==About this Structure==
==About this Structure==
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[[Category: Metap2]]
[[Category: Metap2]]
[[Category: Methionine]]
[[Category: Methionine]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 10:32:20 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 15:33:34 2008''

Revision as of 12:33, 29 July 2008

Image:2oaz.png

Template:STRUCTURE 2oaz

Human Methionine Aminopeptidase-2 Complexed with SB-587094

Template:ABSTRACT PUBMED 17636946

About this Structure

2OAZ is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Highly potent inhibitors of methionine aminopeptidase-2 based on a 1,2,4-triazole pharmacophore., Marino JP Jr, Fisher PW, Hofmann GA, Kirkpatrick RB, Janson CA, Johnson RK, Ma C, Mattern M, Meek TD, Ryan MD, Schulz C, Smith WW, Tew DG, Tomazek TA Jr, Veber DF, Xiong WC, Yamamoto Y, Yamashita K, Yang G, Thompson SK, J Med Chem. 2007 Aug 9;50(16):3777-85. Epub 2007 Jul 18. PMID:17636946

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