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5CN5

Ultrafast dynamics in myoglobin: 0 ps time delay

5CN5 の概要
エントリーDOI10.2210/pdb5cn5/pdb
分子名称Myoglobin, PROTOPORPHYRIN IX CONTAINING FE, SULFATE ION, ... (5 entities in total)
機能のキーワードserial femtosecond crystallography, time-resolved crystallography, free-electron laser, protein dynamics, carbon monoxide, oxygen storage
由来する生物種Equus caballus (Horse)
タンパク質・核酸の鎖数1
化学式量合計17763.09
構造登録者
主引用文献Barends, T.R.,Foucar, L.,Ardevol, A.,Nass, K.,Aquila, A.,Botha, S.,Doak, R.B.,Falahati, K.,Hartmann, E.,Hilpert, M.,Heinz, M.,Hoffmann, M.C.,Kofinger, J.,Koglin, J.E.,Kovacsova, G.,Liang, M.,Milathianaki, D.,Lemke, H.T.,Reinstein, J.,Roome, C.M.,Shoeman, R.L.,Williams, G.J.,Burghardt, I.,Hummer, G.,Boutet, S.,Schlichting, I.
Direct observation of ultrafast collective motions in CO myoglobin upon ligand dissociation.
Science, 350:445-450, 2015
Cited by
PubMed Abstract: The hemoprotein myoglobin is a model system for the study of protein dynamics. We used time-resolved serial femtosecond crystallography at an x-ray free-electron laser to resolve the ultrafast structural changes in the carbonmonoxy myoglobin complex upon photolysis of the Fe-CO bond. Structural changes appear throughout the protein within 500 femtoseconds, with the C, F, and H helices moving away from the heme cofactor and the E and A helices moving toward it. These collective movements are predicted by hybrid quantum mechanics/molecular mechanics simulations. Together with the observed oscillations of residues contacting the heme, our calculations support the prediction that an immediate collective response of the protein occurs upon ligand dissociation, as a result of heme vibrational modes coupling to global modes of the protein.
PubMed: 26359336
DOI: 10.1126/science.aac5492
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.8 Å)
構造検証レポート
Validation report summary of 5cn5
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2025-06-25に公開中

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