3ao5
From Proteopedia
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==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:021275048</ref><references group="xtra"/> |
[[Category: Human immunodeficiency virus 1]] | [[Category: Human immunodeficiency virus 1]] | ||
[[Category: Chalmers, D K.]] | [[Category: Chalmers, D K.]] | ||
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[[Category: Scanlon, M J.]] | [[Category: Scanlon, M J.]] | ||
[[Category: Wielens, J.]] | [[Category: Wielens, J.]] | ||
| + | [[Category: Aid]] | ||
| + | [[Category: Dna binding]] | ||
| + | [[Category: Dna integration]] | ||
| + | [[Category: Endonuclease]] | ||
| + | [[Category: Fragment binding]] | ||
| + | [[Category: Integrase]] | ||
| + | [[Category: Polynucleotidyl transferase]] | ||
| + | [[Category: Rnaseh]] | ||
| + | [[Category: Viral protein]] | ||
| + | [[Category: Viral protein-transferase inhibitor complex]] | ||
Revision as of 13:30, 6 February 2013
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
Categories: Human immunodeficiency virus 1 | Chalmers, D K. | Headey, S J. | Parker, M W. | Scanlon, M J. | Wielens, J. | Aid | Dna binding | Dna integration | Endonuclease | Fragment binding | Integrase | Polynucleotidyl transferase | Rnaseh | Viral protein | Viral protein-transferase inhibitor complex
