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3AO3

Fragment-based approach to the design of ligands targeting a novel site on HIV-1 integrase

Summary for 3AO3
Entry DOI10.2210/pdb3ao3/pdb
Related3AO1 3AO2 3AO4 3AO5 3OVN 3l3u
DescriptorPOL polyprotein, CADMIUM ION, CHLORIDE ION, ... (6 entities in total)
Functional Keywordsdna integration, aids, integrase, endonuclease, polynucleotidyl transferase, dna binding, viral protein, rnaseh, fragment binding, viral protein-transferase inhibitor complex, viral protein/transferase inhibitor
Biological sourceHuman immunodeficiency virus 1
Total number of polymer chains2
Total formula weight37129.64
Authors
Wielens, J.,Headey, S.J.,Parker, M.W.,Chalmers, D.K.,Scanlon, M.J. (deposition date: 2010-09-20, release date: 2011-03-09, Last modification date: 2023-11-01)
Primary citationWielens, J.,Headey, S.J.,Deadman, J.J.,Rhodes, D.I.,Parker, M.W.,Chalmers, D.K.,Scanlon, M.J.
Fragment-based design of ligands targeting a novel site on the integrase enzyme of human immunodeficiency virus 1
Chemmedchem, 6:258-261, 2011
Cited by
PubMed: 21275048
DOI: 10.1002/cmdc.201000483
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

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