3ggx
From Proteopedia
(Difference between revisions)
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+ | [[Image:3ggx.jpg|left|200px]] | ||
- | The | + | <!-- |
+ | The line below this paragraph, containing "STRUCTURE_3ggx", creates the "Structure Box" on the page. | ||
+ | You may change the PDB parameter (which sets the PDB file loaded into the applet) | ||
+ | or the SCENE parameter (which sets the initial scene displayed when the page is loaded), | ||
+ | or leave the SCENE parameter empty for the default display. | ||
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+ | {{STRUCTURE_3ggx| PDB=3ggx | SCENE= }} | ||
- | + | ===HIV Protease, pseudo-symmetric inhibitors=== | |
- | Description: HIV Protease, pseudo-symmetric inhibitors | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May | + | <!-- |
+ | The line below this paragraph, {{ABSTRACT_PUBMED_19323562}}, adds the Publication Abstract to the page | ||
+ | (as it appears on PubMed at http://www.pubmed.gov), where 19323562 is the PubMed ID number. | ||
+ | --> | ||
+ | {{ABSTRACT_PUBMED_19323562}} | ||
+ | |||
+ | ==About this Structure== | ||
+ | 3GGX is a 8 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=3GGX OCA]. | ||
+ | |||
+ | ==Reference== | ||
+ | <ref group="xtra">PMID:19323562</ref><references group="xtra"/> | ||
+ | [[Category: Human immunodeficiency virus 1]] | ||
+ | [[Category: Stoll, V S.]] | ||
+ | [[Category: Hiv protease]] | ||
+ | [[Category: Hydrolase]] | ||
+ | [[Category: Protease]] | ||
+ | [[Category: Pseudo-symmetric inhibitor]] | ||
+ | |||
+ | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed May 27 15:22:02 2009'' |
Revision as of 12:22, 27 May 2009
HIV Protease, pseudo-symmetric inhibitors
Template:ABSTRACT PUBMED 19323562
About this Structure
3GGX is a 8 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Degoey DA, Grampovnik DJ, Flentge CA, Flosi WJ, Chen HJ, Yeung CM, Randolph JT, Klein LL, Dekhtyar T, Colletti L, Marsh KC, Stoll V, Mamo M, Morfitt DC, Nguyen B, Schmidt JM, Swanson SJ, Mo H, Kati WM, Molla A, Kempf DJ. 2-Pyridyl P1'-substituted symmetry-based human immunodeficiency virus protease inhibitors (A-792611 and A-790742) with potential for convenient dosing and reduced side effects. J Med Chem. 2009 Apr 23;52(8):2571-86. PMID:19323562 doi:http://dx.doi.org/10.1021/jm900044w
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