3ao5
From Proteopedia
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| + | {{STRUCTURE_3ao5| PDB=3ao5 | SCENE= }} | ||
| - | + | ===Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase=== | |
| - | Description: Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase | ||
| - | + | ==About this Structure== | |
| + | [[3ao5]] is a 2 chain structure with sequence 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=3AO5 OCA]. | ||
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| + | ==Reference== | ||
| + | <ref group="xtra">PMID:21275048</ref><references group="xtra"/> | ||
| + | [[Category: Human immunodeficiency virus 1]] | ||
| + | [[Category: Chalmers, D K.]] | ||
| + | [[Category: Headey, S J.]] | ||
| + | [[Category: Parker, M W.]] | ||
| + | [[Category: Scanlon, M J.]] | ||
| + | [[Category: Wielens, J.]] | ||
Revision as of 06:26, 9 March 2011
Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase
About this Structure
3ao5 is a 2 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Wielens J, Headey SJ, Deadman JJ, Rhodes DI, Parker MW, Chalmers DK, Scanlon MJ. Fragment-based design of ligands targeting a novel site on the integrase enzyme of human immunodeficiency virus 1. ChemMedChem. 2011 Feb 7;6(2):258-61. doi: 10.1002/cmdc.201000483. Epub, 2010 Dec 16. PMID:21275048 doi:10.1002/cmdc.201000483
