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Crystal structure of human ubiquitous mitochondrial creatine kinase

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Eder,  Michael
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Fritz-Wolf,  Karin
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Kabsch,  Wolfgang
Emeritus Group Biophysics, Max Planck Institute for Medical Research, Max Planck Society;

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Citation

Eder, M., Fritz-Wolf, K., Kabsch, W., Wallimann, T., & Schlattner, U. (2000). Crystal structure of human ubiquitous mitochondrial creatine kinase. Proteins: Structure, Function, and Bioinformatics, 39(3), 216-225. doi:10.1002/(SICI)1097-0134(20000515)39:3<216:AID-PROT40>3.0.CO;2-#.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0027-AE73-D
Abstract
Creatine kinase (CK), catalyzing the reversible trans-phosphorylation between ATP and creatine, plays a key role in the energy metabolism of cells with high and fluctuating energy requirements. We have solved the X-ray structure of octameric human ubiquitous mitochondrial CK (uMtCK) at 2.7 ? resolution, representing the first human CK structure. The structure is very similar to the previously determined structure of sarcomeric mitochondrial CK (sMtCK). The cuboidal octamer has 422 point group symmetry with four dimers arranged along the fourfold axis and a central channel of 20 ? diameter, which extends through the whole octamer. Structural differences with respect to sMtCK are found in isoform-specific regions important for octamer formation and membrane binding. Octameric uMtCK is stabilized by numerous additional polar interactions between the N-termini of neighboring dimers, which extend into the central channel and form clamp-like structures, and by a pair of salt bridges in the hydrophobic interaction patch. The five C-terminal residues of uMtCK, carrying positive charges likely to be involved in phospholipid-binding, are poorly defined by electron density, indicating a more flexible region than the corresponding one in sMtCK. The structural differences between uMtCK and sMtCK are consistent with biochemical studies on octamer stability and membrane binding of the two isoforms