3e0p

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3e0p.jpg|left|200px]]
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The entry 3e0p is ON HOLD until Paper Publication
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{{STRUCTURE_3e0p| PDB=3e0p | SCENE= }}
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Authors: Spraggon, G., Hornsby, M., Shipway, A., Harris, J.L., Lesley, S.A.
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===The X-ray structure of Human Prostasin in complex with a covalent benzoxazole inhibitor===
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Description: The X-ray structure of Human Prostasin in complex with a covalent benzoxazole inhibitor
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Aug 27 10:59:27 2008''
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{{ABSTRACT_PUBMED_18752942}}
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==About this Structure==
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3E0P is a [[Single protein]] structure of 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=3E0P OCA].
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==Reference==
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Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design., Tully DC, Vidal A, Chatterjee AK, Williams JA, Roberts MJ, Petrassi HM, Spraggon G, Bursulaya B, Pacoma R, Shipway A, Schumacher AM, Danahay H, Harris JL, Bioorg Med Chem Lett. 2008 Aug 14. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18752942 18752942]
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[[Category: Homo sapiens]]
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[[Category: Single protein]]
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[[Category: Harris, J L.]]
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[[Category: Hornsby, M.]]
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[[Category: Lesley, S A.]]
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[[Category: Shipway, A.]]
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[[Category: Spraggon, G.]]
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[[Category: Benzoxazole]]
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[[Category: Cell membrane]]
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[[Category: Channel]]
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[[Category: Enac]]
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[[Category: Glycoprotein]]
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[[Category: Hydrolase]]
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[[Category: Membrane]]
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[[Category: Prostasin]]
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[[Category: Protease]]
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[[Category: Secreted]]
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[[Category: Serine protease]]
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[[Category: Transmembrane]]
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[[Category: Warhead]]
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[[Category: Zymogen]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 10 10:36:10 2008''

Revision as of 07:36, 10 September 2008

Image:3e0p.jpg

Template:STRUCTURE 3e0p

The X-ray structure of Human Prostasin in complex with a covalent benzoxazole inhibitor

Template:ABSTRACT PUBMED 18752942

About this Structure

3E0P is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Discovery of inhibitors of the channel-activating protease prostasin (CAP1/PRSS8) utilizing structure-based design., Tully DC, Vidal A, Chatterjee AK, Williams JA, Roberts MJ, Petrassi HM, Spraggon G, Bursulaya B, Pacoma R, Shipway A, Schumacher AM, Danahay H, Harris JL, Bioorg Med Chem Lett. 2008 Aug 14. PMID:18752942

Page seeded by OCA on Wed Sep 10 10:36:10 2008

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OCA

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