2oag
From Proteopedia
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[[Image:2oag.png|left|200px]] | [[Image:2oag.png|left|200px]] | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | [[2oag]] is a 4 chain structure of [[Dipeptidyl peptidase]] with 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=2OAG OCA]. | |
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| + | ==See Also== | ||
| + | *[[Dipeptidyl peptidase]] | ||
==Reference== | ==Reference== | ||
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[[Category: Inhibitor complex]] | [[Category: Inhibitor complex]] | ||
[[Category: Serine-peptidase]] | [[Category: Serine-peptidase]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 17:48:01 2009'' | ||
Revision as of 11:57, 3 January 2011
Contents |
Crystal structure of human dipeptidyl peptidase IV (DPPIV) with pyrrolidine-constrained phenethylamine 29g
Template:ABSTRACT PUBMED 17276063
About this Structure
2oag is a 4 chain structure of Dipeptidyl peptidase with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Reference
- Backes BJ, Longenecker K, Hamilton GL, Stewart K, Lai C, Kopecka H, von Geldern TW, Madar DJ, Pei Z, Lubben TH, Zinker BA, Tian Z, Ballaron SJ, Stashko MA, Mika AK, Beno DW, Kempf-Grote AJ, Black-Schaefer C, Sham HL, Trevillyan JM. Pyrrolidine-constrained phenethylamines: The design of potent, selective, and pharmacologically efficacious dipeptidyl peptidase IV (DPP4) inhibitors from a lead-like screening hit. Bioorg Med Chem Lett. 2007 Apr 1;17(7):2005-12. Epub 2007 Jan 19. PMID:17276063 doi:10.1016/j.bmcl.2007.01.026
