3ao5
From Proteopedia
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
