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Search query: Wilson's disease
9 articles match your search "Wilson's disease"Results 1 to 9, sorted by relevance:
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The modified N-domain of the Wilson disease protein has been crystallized both in its native form and as a selenomethionine derivative. X-ray diffraction data were collected from the native crystal to 1.7 Å resolution, while the selenomethionine derivative diffracted to 2.7 Å resolution.
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Methanobactins are post-translationally modified copper-binding peptides that have a number of potential environmental and biomedical applications. This report presents the crystal structure and preliminary biochemical characterization of the putative methanobactin biosynthesis protein MbnF.
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A PbII coordination polymer was prepared under solvothermal synthetic conditions using the bifunctional ligand 4,4′-(1H,1′H-[2,2′-biimidazole]-1,1′-diyl)dibenzoic acid and Pb(NO3)2. A two-dimensional (2D) coordination network is formed. The central PbII ions adopt distorted octahedral geometries, which are bound by the bifunctional ligand. Furthermore, the 2D coordination layers are assembled into a 3D supramolecular network through hydrogen-bonding interactions. In addition, a fluorescence sensing experiment towards Cu2+ based on the polymeric PbII complex was carried out.
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The anti-apoptotic multidomain protein XIAP is shown to be a compact dimer in solution as determined by an integrative approach combining NMR, SAXS, EPR and molecular modelling.
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A complete set of data is presented, acquired using the Flyscan method after injection of gold-cluster-enriched mesoporous silica nanospheres, used as potential theranostic vectors, into rats.
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Recombinant dipeptidyl peptidase IV from P. gingivalis has been crystallized. Data were collected to 2.7 Å from selenomethionine-derived crystals and structure solution by SAD or MAD is in progress.
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S-Formylglutathione hydrolase has been crystallized and several crystallographic data sets have been collected to a maximum resolution of 1.6 Å. The space group changes from monoclinic C2 to trigonal P3121 or P3221 when the crystal is pressurized in a xenon pressure chamber.
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Progress by the SPINE consortium on the determination of structures of proteins of bacterial and viral pathogens is outlined, with particular reference to the impact of high-throughput technologies.
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The title compound, [Mo2(C5H10NS2)2O4]·C4H8O, can be readily prepared in tetrahydrofuran (THF) by an oxidation reaction between the MoIV precursor [MoO(S2CNEt2)2] with [ReMeO3]. The compound is an axially symmetric MoV dimer (2 symmetry), in which the metal atoms exhibit a distorted square-pyramidal coordination environment. A THF molecule was found to be equally disordered over two symmetry-related sites (around a twofold rotation axis), trans-coordinated to the apical oxido group and weakly interacting with the MoV atoms [Mo—O = 2.6213 (19) Å]. In the crystal, some weak C—H
O interactions occur between the terminal oxido and neighbouring —CH3 groups of an adjacent [Mo(μ-O)O(S2CNEt2)]2 unit.
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