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1TJL

Crystal structure of transcription factor DksA from E. coli

1TJL の概要
エントリーDOI10.2210/pdb1tjl/pdb
分子名称DnaK suppressor protein, ZINC ION (3 entities in total)
機能のキーワードdksa, transcription factor, rna polymerase, stringent response, ppgpp, riken structural genomics/proteomics initiative, rsgi, structural genomics, transcription
由来する生物種Escherichia coli
細胞内の位置Cytoplasm: P0ABS1
タンパク質・核酸の鎖数10
化学式量合計176201.96
構造登録者
主引用文献Perederina, A.,Svetlov, V.,Vassylyeva, M.N.,Tahirov, T.H.,Yokoyama, S.,Artsimovitch, I.,Vassylyev, D.G.
Regulation through the secondary channel--structural framework for ppGpp-DksA synergism during transcription
Cell(Cambridge,Mass.), 118:297-309, 2004
Cited by
PubMed Abstract: Bacterial transcription is regulated by the alarmone ppGpp, which binds near the catalytic site of RNA polymerase (RNAP) and modulates its activity. We show that the DksA protein is a crucial component of ppGpp-dependent regulation. The 2.0 A resolution structure of Escherichia coli DksA reveals a globular domain and a coiled coil with two highly conserved Asp residues at its tip that is reminiscent of the transcript cleavage factor GreA. This structural similarity suggests that DksA coiled coil protrudes into the RNAP secondary channel to coordinate a ppGpp bound Mg2+ ion with the Asp residues, thereby stabilizing the ppGpp-RNAP complex. Biochemical analysis demonstrates that DksA affects transcript elongation, albeit differently from GreA; augments ppGpp effects on initiation; and binds directly to RNAP, positioning the Asp residues near the active site. Substitution of these residues eliminates the synergy between DksA and ppGpp. Thus, the secondary channel emerges as a common regulatory entrance for transcription factors.
PubMed: 15294156
DOI: 10.1016/j.cell.2004.06.030
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 1tjl
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2026-04-29に公開中

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