3L3V
Structure of HIV-1 integrase core domain in complex with sucrose
3L3V の概要
エントリーDOI | 10.2210/pdb3l3v/pdb |
関連するPDBエントリー | 1BL3 1EXQ 3L3U |
関連するBIRD辞書のPRD_ID | PRD_900003 |
分子名称 | POL polyprotein, beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, SULFATE ION, ... (5 entities in total) |
機能のキーワード | dna integration, aids, integrase, endonuclease, polynucleotidyl transferase, dna binding, viral protein |
由来する生物種 | Human immunodeficiency virus 1 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 36588.41 |
構造登録者 | Wielens, J.,Chalmers, D.K.,Scanlon, M.J.,Parker, M.W. (登録日: 2009-12-18, 公開日: 2010-03-31, 最終更新日: 2023-11-01) |
主引用文献 | Wielens, J.,Headey, S.J.,Jeevarajah, D.,Rhodes, D.I.,Deadman, J.,Chalmers, D.K.,Scanlon, M.J.,Parker, M.W. Crystal structure of the HIV-1 integrase core domain in complex with sucrose reveals details of an allosteric inhibitory binding site Febs Lett., 584:1455-1462, 2010 Cited by PubMed Abstract: HIV integrase (IN) is an essential enzyme in HIV replication and an important target for drug design. IN has been shown to interact with a number of cellular and viral proteins during the integration process. Disruption of these important interactions could provide a mechanism for allosteric inhibition of IN. We present the highest resolution crystal structure of the IN core domain to date. We also present a crystal structure of the IN core domain in complex with sucrose which is bound at the dimer interface in a region that has previously been reported to bind integrase inhibitors. PubMed: 20227411DOI: 10.1016/j.febslet.2010.03.016 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2 Å) |
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