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2TRT

TETRACYCLINE REPRESSOR CLASS D

1TRT」から置き換えられました
2TRT の概要
エントリーDOI10.2210/pdb2trt/pdb
分子名称TETRACYCLINE REPRESSOR CLASS D, MAGNESIUM ION, TETRACYCLINE, ... (4 entities in total)
機能のキーワードtranscription regulation, repressor, dna-binding
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24786.35
構造登録者
Hinrichs, W.,Kisker, C.,Saenger, W. (登録日: 1994-03-04, 公開日: 1996-06-20, 最終更新日: 2024-02-21)
主引用文献Hinrichs, W.,Kisker, C.,Duvel, M.,Muller, A.,Tovar, K.,Hillen, W.,Saenger, W.
Structure of the Tet repressor-tetracycline complex and regulation of antibiotic resistance.
Science, 264:418-420, 1994
Cited by
PubMed Abstract: The most frequently occurring resistance of Gram-negative bacteria against tetracyclines is triggered by drug recognition of the Tet repressor. This causes dissociation of the repressor-operator DNA complex and enables expression of the resistance protein TetA, which is responsible for active efflux of tetracycline. The 2.5 angstrom resolution crystal structure of the homodimeric Tet repressor complexed with tetracycline-magnesium reveals detailed drug recognition. The orientation of the operator-binding helix-turn-helix motifs of the repressor is inverted in comparison with other DNA binding proteins. The repressor-drug complex is unable to interact with DNA because the separation of the DNA binding motifs is 5 angstroms wider than usually observed.
PubMed: 8153629
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.5 Å)
構造検証レポート
Validation report summary of 2trt
検証レポート(詳細版)ダウンロードをダウンロード

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件を2025-06-04に公開中

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