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- W1504098090 abstract "Image analysis has been used to compare the projection structure of three-dimensional crystals of (Na+,K+)-ATPase from pig kidney and the Ca(2+)-ATPase from rabbit muscle sarcoplasmic reticulum. These crystals, formed from detergent-solubilized protein in the presence of 20% glycerol and at a low detergent to protein ratio, crystallize in nearly identical unit cells in the space group C2. Average cell dimensions for the Ca(2+)-ATPase were a = 166.8 +/- 4.5 A, b = 57.7 +/- 4.4 A, gamma = 90 degrees while those for the (Na+,K+)-ATPase were a = 166.2 +/- 3.8A, b = 54.25 +/- 3.5A, gamma = 90 degrees. Their projected structures at the resolution of 25-A resolution are indistinguishable. Thus, the (Na+,K+)-ATPase crystals appear to contain only the alpha chain of the alpha beta heterodimer found in native membranes. We conclude from this that the three-dimensional structure of the alpha chain of the (Na+,K+)-ATPase is very similar to that of the Ca(2+)-ATPase despite their relatively weak overall sequence homology." @default.
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- W1504098090 date "1994-04-01" @default.
- W1504098090 modified "2023-10-18" @default.
- W1504098090 title "Similarity of three-dimensional microcrystals of detergent-solubilized (Na+,K+)-ATPase from pig kidney and Ca(2+)-ATPase from skeletal muscle sarcoplasmic reticulum" @default.
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- W1504098090 doi "https://doi.org/10.1016/s0021-9258(17)36996-x" @default.
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