5JDT
Structure of Spin-labelled T4 lysozyme mutant L118C-R1 at 100K
5JDT の概要
エントリーDOI | 10.2210/pdb5jdt/pdb |
分子名称 | Endolysin, S-[(1-oxyl-2,2,5,5-tetramethyl-2,5-dihydro-1H-pyrrol-3-yl)methyl] methanesulfonothioate, CHLORIDE ION, ... (7 entities in total) |
機能のキーワード | nitroxide, spin label, t4 lysozyme, electron paramagnetic resonance, hydrolase |
由来する生物種 | Enterobacteria phage T4 |
細胞内の位置 | Host cytoplasm : P00720 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 19190.36 |
構造登録者 | Loll, B.,Consentius, P.,Gohlke, U.,Mueller, R.,Kaupp, M.,Heinemann, U.,Wahl, M.C.,Risse, T. (登録日: 2016-04-17, 公開日: 2016-09-28, 最終更新日: 2024-04-03) |
主引用文献 | Consentius, P.,Gohlke, U.,Loll, B.,Alings, C.,Muller, R.,Heinemann, U.,Kaupp, M.,Wahl, M.,Risse, T. Tracking Transient Conformational States of T4 Lysozyme at Room Temperature Combining X-ray Crystallography and Site-Directed Spin Labeling. J.Am.Chem.Soc., 138:12868-12875, 2016 Cited by PubMed Abstract: Proteins are dynamic molecules that can transiently adopt different conformational states. As the function of the system often depends critically on its conformational state a rigorous understanding of the correlation between structure, energetics and dynamics of the different accessible states is crucial. The biophysical characterization of such processes is, however, challenging as the excited states are often only marginally populated. We show that a combination of X-ray crystallography performed at 100 K as well as at room temperature and EPR spectroscopy on a spin-labeled single crystal allows to correlate the structures of the ground state and a thermally excited state with their thermodynamics using the variant 118R1 of T4 lysozyme as an example. In addition, it is shown that the surrounding solvent can significantly alter the energetic as well as the entropic contribution to the Gibbs free energy without major impact on the structure of both states. PubMed: 27673570DOI: 10.1021/jacs.6b05507 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1 Å) |
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