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4NC8

N-terminal domain of delta-subunit of RNA polymerase complexed with nickel ions

4NC8 の概要
エントリーDOI10.2210/pdb4nc8/pdb
関連するPDBエントリー2KRC 4NC7
分子名称DNA-directed RNA polymerase subunit delta, NICKEL (II) ION (3 entities in total)
機能のキーワードnucleus, transcription
由来する生物種Bacillus Subtilis
タンパク質・核酸の鎖数2
化学式量合計23655.55
構造登録者
Demo, G.,Papouskova, V.,Komarek, J.,Sanderova, H.,Rabatinova, A.,Krasny, L.,Zidek, L.,Sklenar, V.,Wimmerova, M. (登録日: 2013-10-24, 公開日: 2014-07-02, 最終更新日: 2023-09-20)
主引用文献Demo, G.,Papouskova, V.,Komarek, J.,Kaderavek, P.,Otrusinova, O.,Srb, P.,Rabatinova, A.,Krasny, L.,Zidek, L.,Sklenar, V.,Wimmerova, M.
X-ray vs. NMR structure of N-terminal domain of delta-subunit of RNA polymerase.
J.Struct.Biol., 187:174-186, 2014
Cited by
PubMed Abstract: The crystal structure of the N-terminal domain of the RNA polymerase δ subunit (Nδ) from Bacillus subtilis solved at a resolution of 2.0Å is compared with the NMR structure determined previously. The molecule crystallizes in the space group C222(1) with a dimer in the asymmetric unit. Importantly, the X-ray structure exhibits significant differences from the lowest energy NMR structure. In addition to the overall structure differences, structurally important β sheets found in the NMR structure are not present in the crystal structure. We systematically investigated the cause of the discrepancies between the NMR and X-ray structures of Nδ, addressing the pH dependence, presence of metal ions, and crystal packing forces. We convincingly showed that the crystal packing forces, together with the presence of Ni(2+) ions, are the main reason for such a difference. In summary, the study illustrates that the two structural approaches may give unequal results, which need to be interpreted with care to obtain reliable structural information in terms of biological relevance.
PubMed: 24937760
DOI: 10.1016/j.jsb.2014.06.001
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.17 Å)
構造検証レポート
Validation report summary of 4nc8
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2025-07-16に公開中

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