U2 and U6 snRNAs pair to form a phylogenetically conserved complex at the catalytic core of the spliceosome. Interactions with divalent metal ions, particularly Mg(II), at specific sites are essential for its folding and catalytic activity. We used a novel Förster resonance energy transfer (FRET) method between site-bound luminescent lanthanide ions and a covalently attached fluorescent dye, co...

The structure of 3',5'-thymidine diphosphate bound in the active site of staphylococcal nuclease (EC 3.1.4.7) was studied by measuring the relaxation rate enhancement of substrate analog nuclei by a paramagnetic metal ion. The lanthanide ion, Gd(III), was substituted for Ca(II) in the formation of the ternary complex of nuclease-Gd(III)-3',5'-thymidine diphosphate. Measurements were made of the...

Isostructural vanadium, niobium and tantalum complexes of bis(3,5-di-tert-butyl-2-phenol)amine ([ONO]H3), were prepared and characterized to evaluate the impact of the metal ion on redox-activity of the ligand platform. New vanadium and niobium complexes with the general formula, [ONO]MCl2L (M = V, L = THF, 1-V; M = Nb, L = Et2O, 1-Nb) were prepared and structurally analysed by X-ray crystallog...

U2 and U6 snRNAs pair to form a phylogenetically conserved complex at the catalytic core of the spliceosome. Interactions with divalent metal ions, particularly Mg(II), at specific sites are essential for its folding and catalytic activity. We used a novel Förster resonance energy transfer (FRET) method between site-bound luminescent lanthanide ions and a covalently attached fluorescent dye, co...

salicylic acid-formaldehyde-m-cresol (sfm) terpolymer had been synthesized in dmf media by conventional method. the resulting resin had been characterized by ftir spectra, elemental and thermogravimetric analyses. the morphology of sfm resin had been studied by sem and optical photograph. various parameters like rate of equilibration, effect of ph on ion exchange capacity and effect of concentr...

In the title complex, [Cd(C12H11N4S2)I(C12H12N4S2)], the Cd(II) ion is penta-coordinated by two thio-semicarbazone ligands (one neutral and the other anionic) and one iodide ion in a distorted square pyramidal (τ = 0.35) geometry. The central ion is coordinated by the thia-zole N atom, the thio-ureido N and the S atom of the deprotonated thio-semicarbazone ligand. The other ligand is linked wit...

The solvation of the ruthenium(II) tris(bipyridine) ion ([Ru(bpy)3](2+)) is investigated with molecular dynamics simulations of lithium halide solutions in polar solvents. The anion distribution around the [Ru(bpy)3](2+) complex exhibits a strong solvent dependence. In aqueous solution, the iodide ion forms a solvent shared complex with [Ru(bpy)3](2+), but not in the other solvents. Between Cl(...

A specific class of anions inhibit creatine kinase by stabilizing the dead-end complex, enzymedivalent cation*ADP*creatine (Watts, D. C. (1973) The Enzymes 8, 383-455). The inhibitory action o? the anions is attributed to the ability of the anions to mimic the equatorial PO3 plane formed by the migrating phosphoryl group in the transition state of the reaction. Infrared spectroscopy has been us...

(Full text is available at http://www.manu.edu.mk/prilozi). IR spectroscopy was used to follow the dynamic structural transitions of the transfection competent 100 nm DNA-divalent metal cation-phospholipid ternary complex upon recognition of individual molecules engaged. The selection of small charged metal ions as complexing agents and zwitterionic L-alpha-phosphatidylcholine as an alternative...

BphH is a divalent metal ion-dependent hydratase that catalyzes the formation of 2-keto-4-hydroxypentanoate from 2-hydroxypent-2,4-dienoate (HPDA). This reaction lies on the catabolic pathway of numerous aromatics, including the significant environmental pollutant, polychlorinated biphenyls (PCBs). BphH from the PCB degrading bacterium, Burkholderia xenoverans LB400, was overexpressed and purif...