3e16
From Proteopedia
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+ | [[Image:3e16.jpg|left|200px]] | ||
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+ | The line below this paragraph, containing "STRUCTURE_3e16", creates the "Structure Box" on the page. | ||
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+ | {{STRUCTURE_3e16| PDB=3e16 | SCENE= }} | ||
- | + | ===X-ray structure of human prostasin in complex with Benzoxazole warhead peptidomimic, lysine in P3=== | |
- | Description: X-ray structure of human prostasin in complex with Benzoxazole warhead peptidomimic, lysine in P3 | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_18752942}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 18752942 is the PubMed ID number. | ||
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+ | {{ABSTRACT_PUBMED_18752942}} | ||
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+ | ==About this Structure== | ||
+ | 3E16 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=3E16 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:[http://www.ncbi.nlm.nih.gov/pubmed/18752942 18752942] | ||
+ | [[Category: Homo sapiens]] | ||
+ | [[Category: Single protein]] | ||
+ | [[Category: Harris, J L.]] | ||
+ | [[Category: Hornsby, M.]] | ||
+ | [[Category: Lesley, S A.]] | ||
+ | [[Category: Shipway, A.]] | ||
+ | [[Category: Spraggon, G.]] | ||
+ | [[Category: Benzoxazole]] | ||
+ | [[Category: Cell membrane]] | ||
+ | [[Category: Channel activating protease]] | ||
+ | [[Category: Enac]] | ||
+ | [[Category: Glycoprotein]] | ||
+ | [[Category: Hcap-1]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Inhibitor]] | ||
+ | [[Category: Membrane]] | ||
+ | [[Category: Prostasin]] | ||
+ | [[Category: Protease]] | ||
+ | [[Category: Secreted]] | ||
+ | [[Category: Serine protease]] | ||
+ | [[Category: Transmembrane]] | ||
+ | [[Category: Zymogen]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Sep 10 10:33:53 2008'' |
Revision as of 07:33, 10 September 2008
X-ray structure of human prostasin in complex with Benzoxazole warhead peptidomimic, lysine in P3
Template:ABSTRACT PUBMED 18752942
About this Structure
3E16 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 10:33:53 2008
Categories: Homo sapiens | Single protein | Harris, J L. | Hornsby, M. | Lesley, S A. | Shipway, A. | Spraggon, G. | Benzoxazole | Cell membrane | Channel activating protease | Enac | Glycoprotein | Hcap-1 | Hydrolase | Inhibitor | Membrane | Prostasin | Protease | Secreted | Serine protease | Transmembrane | Zymogen