Hatti, Kaushik and Mathiharan, Yamuna Kalyani and Srinivasan, Narayanaswamy and Murthy, Mathur RN (2017) Seeing but not believing: the structure of glycerol dehydrogenase initially assumed to be the structure of a survival protein fromSalmonella typhimurium. In: Acta Crystallographica Section D Structural Biology, 73 (7). pp. 609-617. ISSN 2059-7983
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Abstract
The determination of the crystal structure of a mutant protein using phases based on a previously determined crystal structure of the wild-type protein is often a straightforward molecular-replacement protocol. Such a structure determination may be difficult if there are large-scale structural differences between the wild-type and mutant proteins. In this manuscript, an interesting case is presented of the unintentional crystallization of a contaminant protein which shared some structural features with the presumed target protein, leading to difficulties in obtaining a completely satisfactory molecular-replacement structure solution. It was not immediately evident that the initial structure solution was incorrect owing to the poor quality of the X-ray diffraction data and low resolution. The structure was subsequently determined by improving the quality of the data and following a sequence-independent MarathonMR protocol. The structure corresponded to that of glycerol dehydrogenase, which crystallized as a contaminant, instead of the presumed mutant of a survival protein encoded by Salmonella typhimurium. The reasons why a solution that appeared to be reasonable was obtained with an incorrect protein model are discussed. The results presented here show that a degree of caution is warranted when handling large-scale structure-determination projects.A seemingly reasonable solution was obtained for the structure of a presumed mutant of an S. typhimurium survival protein (SurE) by molecular replacement using the wild-type SurE structure as the phasing model. Although the crystal was of glycerol dehydrogenase, as subsequently demonstrated using the MarathonMR protocol, the initial structure appeared to be reasonable because of a partial similarity in the arrangement of secondary-structural elements in the two proteins.
Item Type: | Journal Article |
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Publication: | Acta Crystallographica Section D Structural Biology |
Publisher: | International Union of Crystallography |
Additional Information: | The copyright for this article belongs to the International Union of Crystallography. |
Keywords: | contaminant; glycerol dehydrogenase; MarathonMR; molecular replacement; serendipity |
Department/Centre: | Division of Biological Sciences > Molecular Biophysics Unit |
Date Deposited: | 08 Jun 2022 05:25 |
Last Modified: | 08 Jun 2022 05:25 |
URI: | https://eprints.iisc.ac.in/id/eprint/73157 |
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