5ED4
Structure of a PhoP-DNA complex
5ED4 の概要
| エントリーDOI | 10.2210/pdb5ed4/pdb |
| 分子名称 | Response regulator, DNA (26-MER), CALCIUM ION, ... (7 entities in total) |
| 機能のキーワード | protein-dna complex, winged helix-turn-helix, direct repeat, tandem dimer, transcription-dna complex, transcription/dna |
| 由来する生物種 | Mycobacterium tuberculosis 詳細 |
| タンパク質・核酸の鎖数 | 8 |
| 化学式量合計 | 143959.57 |
| 構造登録者 | |
| 主引用文献 | He, X.,Wang, L.,Wang, S. Structural basis of DNA sequence recognition by the response regulator PhoP in Mycobacterium tuberculosis. Sci Rep, 6:24442-24442, 2016 Cited by PubMed Abstract: The transcriptional regulator PhoP is an essential virulence factor in Mycobacterium tuberculosis, and it presents a target for the development of new anti-tuberculosis drugs and attenuated tuberculosis vaccine strains. PhoP binds to DNA as a highly cooperative dimer by recognizing direct repeats of 7-bp motifs with a 4-bp spacer. To elucidate the PhoP-DNA binding mechanism, we determined the crystal structure of the PhoP-DNA complex. The structure revealed a tandem PhoP dimer that bound to the direct repeat. The surprising tandem arrangement of the receiver domains allowed the four domains of the PhoP dimer to form a compact structure, accounting for the strict requirement of a 4-bp spacer and the highly cooperative binding of the dimer. The PhoP-DNA interactions exclusively involved the effector domain. The sequence-recognition helix made contact with the bases of the 7-bp motif in the major groove, and the wing interacted with the adjacent minor groove. The structure provides a starting point for the elucidation of the mechanism by which PhoP regulates the virulence of M. tuberculosis and guides the design of screening platforms for PhoP inhibitors. PubMed: 27079268DOI: 10.1038/srep24442 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2.4 Å) |
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