5FKL
TetR(D) H100A mutant in complex with anhydrotetracycline and magnesium
5FKL の概要
| エントリーDOI | 10.2210/pdb5fkl/pdb |
| 関連するPDBエントリー | 5FKK 5FKM 5FKN 5FKO |
| 分子名称 | TETRACYCLINE REPRESSOR, CLASS D, 5A,6-ANHYDROTETRACYCLINE, MAGNESIUM ION, ... (6 entities in total) |
| 機能のキーワード | transcription, repressor, antibiotic resistance, tetr |
| 由来する生物種 | ESCHERICHIA COLI |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 23874.41 |
| 構造登録者 | Werten, S.,Schneider, J.,Palm, G.J.,Hinrichs, W. (登録日: 2015-10-17, 公開日: 2016-04-06, 最終更新日: 2024-01-10) |
| 主引用文献 | Werten, S.,Schneider, J.,Palm, G.J.,Hinrichs, W. Modular Organisation of Inducer Recognition and Allostery in the Tetracycline Repressor FEBS J., 283:2102-, 2016 Cited by PubMed Abstract: Induction of the tetracycline repressor (TetR) results from antibiotic-dependent changes in the relative positioning of the DNA-binding domains within the promoter-associated repressor dimer, but the key determinants of this allosteric effect remain poorly characterised. Intriguingly, previous mutational analyses of the tetracycline-interacting site revealed a lack of correlation between residual affinity and induction propensity, suggesting that some of the residues in contact with the antibiotic primarily act in ligand recognition and retention, whereas others are required to transmit the allosteric signal. Here, we provide a structural basis for these observations via crystallographic analysis of the point mutants N82A, H100A, T103A and E147A in complex with the inducer 5a,6-anhydrotetracycline. In conjunction with the available functional data, the four structures demonstrate that a trigger-like movement of the region between helices α6 and α7 towards and into the binding site plays a decisive role in the intramolecular communication process. In sharp contrast, residues lining the binding cavity proper have little or no influence on the allosteric mechanism as such. This nearly complete physical separation of ligand recognition and allostery will have allowed diverging TetR-like repressors to bind novel effectors while the existing induction mechanism remained intact. Consequently, the modularity described here may have been a key factor in the evolutionary success of the widespread and highly diversified repressor class. PubMed: 27028290DOI: 10.1111/FEBS.13723 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.9 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






