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4NN1

Crystal Structure of transcriptional regulator Rv1219c of Mycobacterium tuberculosis

4NN1 の概要
エントリーDOI10.2210/pdb4nn1/pdb
分子名称Transcriptional regulator (1 entity in total)
機能のキーワードhelix turn helix motif, dna binding transcriptional regulator, dna binding, transcription
由来する生物種Mycobacterium tuberculosis
タンパク質・核酸の鎖数1
化学式量合計24040.26
構造登録者
Kumar, N.,Radhakrishnan, A.,Chou, T.-H.,Yu, E. (登録日: 2013-11-15, 公開日: 2014-02-19, 最終更新日: 2024-02-28)
主引用文献Kumar, N.,Radhakrishnan, A.,Wright, C.C.,Chou, T.H.,Lei, H.T.,Bolla, J.R.,Tringides, M.L.,Rajashankar, K.R.,Su, C.C.,Purdy, G.E.,Yu, E.W.
Crystal structure of the transcriptional regulator Rv1219c of Mycobacterium tuberculosis.
Protein Sci., 23:423-432, 2014
Cited by
PubMed Abstract: The Rv1217c-Rv1218c multidrug efflux system, which belongs to the ATP-binding cassette superfamily, recognizes and actively extrudes a variety of structurally unrelated toxic chemicals and mediates the intrinsic resistance to these antimicrobials in Mycobacterium tuberculosis. The expression of Rv1217c-Rv1218c is controlled by the TetR-like transcriptional regulator Rv1219c, which is encoded by a gene immediately upstream of rv1218c. To elucidate the structural basis of Rv1219c regulation, we have determined the crystal structure of Rv1219c, which reveals a dimeric two-domain molecule with an entirely helical architecture similar to members of the TetR family of transcriptional regulators. The N-terminal domains of the Rv1219c dimer are separated by a large center-to-center distance of 64 Å. The C-terminal domain of each protomer possesses a large cavity. Docking of small compounds to Rv1219c suggests that this large cavity forms a multidrug binding pocket, which can accommodate a variety of structurally unrelated antimicrobial agents. The internal wall of the multidrug binding site is surrounded by seven aromatic residues, indicating that drug binding may be governed by aromatic stacking interactions. In addition, fluorescence polarization reveals that Rv1219c binds drugs in the micromolar range.
PubMed: 24424575
DOI: 10.1002/pro.2424
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.99 Å)
構造検証レポート
Validation report summary of 4nn1
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2025-12-31に公開中

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