3iej
From Proteopedia
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| + | [[Image:3iej.jpg|left|200px]] | ||
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| + | The line below this paragraph, containing "STRUCTURE_3iej", creates the "Structure Box" on the page. | ||
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| + | {{STRUCTURE_3iej| PDB=3iej | SCENE= }} | ||
| - | + | ===Pyrazole-based Cathepsin S Inhibitors with Arylalkynes as P1 Binding Elements=== | |
| - | Description: Pyrazole-based Cathepsin S Inhibitors with Arylalkynes as P1 Binding Elements | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_19773165}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 19773165 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_19773165}} | ||
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| + | ==About this Structure== | ||
| + | 3IEJ is a 2 chains structure of sequences 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=3IEJ OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:19773165</ref><references group="xtra"/> | ||
| + | [[Category: Cathepsin S]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Bembenek, S.]] | ||
| + | [[Category: Cathepsin s]] | ||
| + | [[Category: Disulfide bond]] | ||
| + | [[Category: Glycoprotein]] | ||
| + | [[Category: Hydrolase]] | ||
| + | [[Category: Lysosome]] | ||
| + | [[Category: Polymorphism]] | ||
| + | [[Category: Protease]] | ||
| + | [[Category: Thiol protease]] | ||
| + | [[Category: Zymogen]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 7 13:55:39 2009'' | ||
Revision as of 11:55, 7 October 2009
Pyrazole-based Cathepsin S Inhibitors with Arylalkynes as P1 Binding Elements
Template:ABSTRACT PUBMED 19773165
About this Structure
3IEJ is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Ameriks MK, Axe FU, Bembenek SD, Edwards JP, Gu Y, Karlsson L, Randal M, Sun S, Thurmond RL, Zhu J. Pyrazole-based cathepsin S inhibitors with arylalkynes as P1 binding elements. Bioorg Med Chem Lett. 2009 Nov 1;19(21):6131-4. Epub 2009 Sep 10. PMID:19773165 doi:10.1016/j.bmcl.2009.09.014
Page seeded by OCA on Wed Oct 7 13:55:39 2009
Categories: Cathepsin S | Homo sapiens | Bembenek, S. | Cathepsin s | Disulfide bond | Glycoprotein | Hydrolase | Lysosome | Polymorphism | Protease | Thiol protease | Zymogen
