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The preparation and crystal structure determination of the active-site Cys25→Ser mutant of human cathepsin S at 2.2 Å resolution is described. This structure clearly defines both the catalytic triad and the substrate-binding region.

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The ATPase domain of the membrane-anchored protease FtsH of E. coli has been crystallized and native data to 1.5 Å spacing have been collected using synchrotron radiation.
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