4TSX
HIV-1 Integrase Catalytic Core Domain Mutant Complexed with Allosteric Inhibitor
Summary for 4TSX
Entry DOI | 10.2210/pdb4tsx/pdb |
Related | 1ITG |
Descriptor | Integrase, (2S)-tert-butoxy[4-(3,4-dihydro-2H-chromen-6-yl)-2-methylquinolin-3-yl]ethanoic acid, SULFATE ION, ... (4 entities in total) |
Functional Keywords | hiv integrase, ccd, h171t, dde motif, dimer interface, allosteric inhibitor, allini, quinoline, dna binding protein |
Biological source | Human immunodeficiency virus 1 |
Total number of polymer chains | 1 |
Total formula weight | 18713.01 |
Authors | Feng, L.,Kvaratskhelia, M. (deposition date: 2014-06-19, release date: 2014-12-17, Last modification date: 2023-12-27) |
Primary citation | Slaughter, A.,Jurado, K.A.,Deng, N.,Feng, L.,Kessl, J.J.,Shkriabai, N.,Larue, R.C.,Fadel, H.J.,Patel, P.A.,Jena, N.,Fuchs, J.R.,Poeschla, E.,Levy, R.M.,Engelman, A.,Kvaratskhelia, M. The mechanism of H171T resistance reveals the importance of N -protonated His171 for the binding of allosteric inhibitor BI-D to HIV-1 integrase. Retrovirology, 11:100-100, 2014 Cited by PubMed: 25421939DOI: 10.1186/s12977-014-0100-1 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.94 Å) |
Structure validation
Download full validation report