2fdd
From Proteopedia
(Difference between revisions)
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==About this Structure== | ==About this Structure== | ||
- | 2FDD is a | + | 2FDD is a 2 chains structure of sequences from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FDD OCA]. |
==Reference== | ==Reference== | ||
- | + | <ref group="xtra">PMID:16458505</ref><references group="xtra"/> | |
[[Category: HIV-1 retropepsin]] | [[Category: HIV-1 retropepsin]] | ||
[[Category: Human immunodeficiency virus 1]] | [[Category: Human immunodeficiency virus 1]] | ||
- | [[Category: Single protein]] | ||
[[Category: Xu, R X.]] | [[Category: Xu, R X.]] | ||
[[Category: Hiv protease]] | [[Category: Hiv protease]] | ||
[[Category: Inhibitor]] | [[Category: Inhibitor]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 05:45:08 2009'' |
Revision as of 03:45, 17 February 2009
Crystal structure of HIV protease D545701 bound with GW0385
Template:ABSTRACT PUBMED 16458505
About this Structure
2FDD is a 2 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Miller JF, Andrews CW, Brieger M, Furfine ES, Hale MR, Hanlon MH, Hazen RJ, Kaldor I, McLean EW, Reynolds D, Sammond DM, Spaltenstein A, Tung R, Turner EM, Xu RX, Sherrill RG. Ultra-potent P1 modified arylsulfonamide HIV protease inhibitors: the discovery of GW0385. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1788-94. Epub 2006 Feb 3. PMID:16458505 doi:10.1016/j.bmcl.2006.01.035
Page seeded by OCA on Tue Feb 17 05:45:08 2009