5BMP
Crystal Structure of Phosphoglucomutase from Xanthomonas citri complexed with glucose-1-phosphate
Summary for 5BMP
Entry DOI | 10.2210/pdb5bmp/pdb |
Related | 5BMN 5BMR |
Descriptor | Phosphoglucomutase, 1-O-phosphono-alpha-D-glucopyranose, MAGNESIUM ION, ... (4 entities in total) |
Functional Keywords | phosphoglucomutase citrus canker, isomerase |
Biological source | Xanthomonas axonopodis pv. citri (strain 306) |
Total number of polymer chains | 1 |
Total formula weight | 51501.91 |
Authors | Goto, L.S.,Pereira, H.M.,Novo Mansur, M.T.M. (deposition date: 2015-05-22, release date: 2016-06-01, Last modification date: 2024-11-20) |
Primary citation | Goto, L.S.,Vessoni Alexandrino, A.,Malvessi Pereira, C.,Silva Martins, C.,D'Muniz Pereira, H.,Brandao-Neto, J.,Marques Novo-Mansur, M.T. Structural and functional characterization of the phosphoglucomutase from Xanthomonas citri subsp. citri. Biochim.Biophys.Acta, 1864:1658-1666, 2016 Cited by PubMed Abstract: Citrus canker, caused by bacteria Xanthomonas citri subsp. citri, can affect all economically important varieties of citrus. Studying Xanthomonas genes related to the invasive capacity may improve the knowledge on how this works and ultimately use the information to avoid the disease. Some annotated genes from Xanthomonas citri subsp. citri published genome are addressed to an interesting class of genes named "pathogenicity, virulence and adaptation". One of them is xanA, which encodes a predicted phosphoglucomutase. Phosphoglucomutases are ubiquitous enzymes among the living kingdoms that play roles in carbohydrate metabolism, catalyzing the reversible conversion of 1- to 6-phosphoglucose. In Xanthomonas, phosphoglucomutase activity is required to synthesize precursors of the pathogenesis-related polysaccharide xanthan. In this work, a characterization of this gene product is presented by structural and functional studies. Molecular cloning was used for heterologous expression and deletion of xanA. A Michaelis-Menten kinetics model was obtained using the recombinant protein. The protein structure was also determined by X-ray diffraction on the recombinant enzyme substrate-free, bound to glucose-1,6-biphosphate and to glucose-1-phosphate. Deletion of xanA was done with a suicide plasmid construct and the obtained mutant was tested for pathogenic capacity. This study is the first describing the properties of the Xanthomonas citri subsp. citri phosphoglucomutase. PubMed: 27567706DOI: 10.1016/j.bbapap.2016.08.014 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.85 Å) |
Structure validation
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