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2H3C

Structural basis for nucleic acid and toxin recognition of the bacterial antitoxin CcdA

2H3C の概要
エントリーDOI10.2210/pdb2h3c/pdb
関連するPDBエントリー2H3A
分子名称5'-D(P*AP*TP*AP*TP*GP*TP*AP*TP*AP*CP*CP*CP*G)-3', 5'-D(P*TP*CP*GP*GP*GP*TP*AP*TP*AP*CP*AP*TP*A)-3', CcdA (3 entities in total)
機能のキーワードribbon-helix-helix, immune system-dna complex, immune system/dna
由来する生物種Escherichia coli
タンパク質・核酸の鎖数4
化学式量合計24762.08
構造登録者
Madl, T.,Van Melderen, L.,Respondek, M.,Oberer, M.,Keller, W.,Zangger, K. (登録日: 2006-05-22, 公開日: 2006-11-21, 最終更新日: 2024-05-29)
主引用文献Madl, T.,Van Melderen, L.,Mine, N.,Respondek, M.,Oberer, M.,Keller, W.,Khatai, L.,Zangger, K.
Structural Basis for Nucleic Acid and Toxin Recognition of the Bacterial Antitoxin CcdA
J.Mol.Biol., 364:170-185, 2006
Cited by
PubMed Abstract: Toxin-antitoxin systems are highly abundant in plasmids and bacterial chromosomes. They ensure plasmid maintenance by killing bacteria that have lost the plasmid. Their expression is autoregulated at the level of transcription. Here, we present the solution structure of CcdA, the antitoxin of the ccd system, as a free protein (16.7 kDa) and in complex with its cognate DNA (25.3 kDa). CcdA is composed of two distinct and independent domains: the N-terminal domain, responsible for DNA binding, which establishes a new family of the ribbon-helix-helix fold and the C-terminal region, which is responsible for the interaction with the toxin CcdB. The C-terminal domain is intrinsically unstructured and forms a tight complex with the toxin. We show that CcdA specifically recognizes a 6 bp palindromic DNA sequence within the operator-promoter (OP) region of the ccd operon and binds to DNA by insertion of the positively charged N-terminal beta-sheet into the major groove. The binding of up to three CcdA dimers to a 33mer DNA of its operator-promoter region was studied by NMR spectroscopy, isothermal titration calorimetry and single point mutation. The highly flexible C-terminal region of free CcdA explains its susceptibility to proteolysis by the Lon ATP-dependent protease.
PubMed: 17007877
DOI: 10.1016/j.jmb.2006.08.082
主引用文献が同じPDBエントリー
実験手法
SOLUTION NMR
構造検証レポート
Validation report summary of 2h3c
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2025-06-18に公開中

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