@inproceedings{MaySteinkeMeyer2004, author = {May, Patrick and Steinke, Thomas and Meyer, Michael}, title = {THESEUS: A Parallel Threading Core}, series = {Procs. 12th Internat. Conf. on Intelligent Systems for Mol. Bio. (ISMB) and 3rd European Conf. on Comp. Bio. (ECCB), Glasgow}, booktitle = {Procs. 12th Internat. Conf. on Intelligent Systems for Mol. Bio. (ISMB) and 3rd European Conf. on Comp. Bio. (ECCB), Glasgow}, pages = {199}, year = {2004}, language = {en} } @article{MeyerSteinkeSuehnel2007, author = {Meyer, Michael and Steinke, Thomas and S{\"u}hnel, J{\"u}rgen}, title = {Density functional study of isoguanine tetrad and pentad sandwich complexes with alkali metal ions}, series = {Journal of Molecular Modeling}, volume = {13}, journal = {Journal of Molecular Modeling}, number = {2}, publisher = {Springer Berlin / Heidelberg}, pages = {335 -- 345}, year = {2007}, language = {en} } @misc{MeyerSteinkeBrandletal., author = {Meyer, Michael and Steinke, Thomas and Brandl, Maria and S{\"u}hnel, J{\"u}rgen}, title = {Density functional study of guanine and uracil quartets and of guanine quartet metal/ion complexes}, url = {http://nbn-resolving.de/urn:nbn:de:0297-zib-5842}, number = {00-16}, abstract = {The structures and interaction energies of guanine and uracil quartets have been determined by B3LYP hybrid density functional calculations. The total interaction energy \$\Delta\$E\$^{T}\$ of the \$\it{C}\$\$_{4h}\$-symmetric guanine quartet consisting of Hoogsteen type base pairs with two hydrogen bonds between two neighbour bases is -66.07 kcal/mol at the highest level. The uracil quartet with C6-H6...O4 interactions between the individual bases has only a small interaction energy of -20.92 kcal/mol and the interaction energy of -24.63 kcal/mol for the alternative structure with N3-H3...O4 hydrogen bonds is only slightly more negative. Cooperative effects contribute between 10 and 25 \\% to all interaction energies. Complexes of metal ions with G-quartets can be classified into different structure types. The one with Ca\$^{2+}\$ in the central cavity adopts a \$\it{C}\$\$_{4h}\$-symmetric structure with coplanar bases, whereas the energies of the planar and non-planar Na\$^{+}\$ complexes are almost identical. The small ions Li\$^{+}\$, Be\$^{2+}\$, Cu\$^{+}\$ and Zn\$^{2+}\$ prefer a non-planar \$\it{S}\$\$_{4}\$-symmetric structure. The lack of co-planarity prevents probably a stacking of these base quartets. The central cavity is too small for K\$^{+}\$ ions and therefore this ion favours in contrast to all other investigated ions a \$\it{C}\$\$_{4}\$-symmetric complex, which is 4.73 kcal/mol more stable than the \$\it{C}\$\$_{4h}\$-symmetric one. The distance 1.665 {\AA} between K\$^{+}\$ and the root mean squares plane of the guanine bases is approximately half of the distance between two stacked G-quartets. The total interaction energy of alkaline earth ion complexes exceeds the ones with alkali ions. Within both groups of ions the interaction energy decreases with an increasing row position in the periodic table. The B3LYP and BLYP methods lead to similar structures and energies. Both methods are suitable for hydrogen-bonded biological systems. Compared with the before mentioned methods the HCTH functional leads to longer hydrogen bonds and different relative energies for two U-quartets. Finally we calculated also structures and relative energies with the MMFF94 forcefield. Contrary to all DFT methods, MMFF94 predicts bifurcated C-H...O contacts in the uracil quartet. In the G-quartet the MMFF94 hydrogen bond distances N2-H22...N7 are shorter than the DFT distances, whereas the N1-H1...O6 distances are longer.}, language = {en} } @misc{MeyerSchnurreReissbrodtetal., author = {Meyer, Michael and Schnurre, R{\"u}diger and Reissbrodt, Rolf and Trowitzsch-Kienast, Wolfram}, title = {Computer-aided design of novel siderophores: Pyridinochelin}, url = {http://nbn-resolving.de/urn:nbn:de:0297-zib-5887}, number = {00-20}, abstract = {Pyridinochelin, a novel catecholate type siderophore, has been designed on the basis of the active analog enterobactin. Growth promotion tests indicate that this synthetic siderophore feeds various pathogenic bacteria effectively with iron even though it lacks one catecholate group compared to enterobactin. The superposition of the siderophore structures suggests that the structure of the skeleton connecting the catecholate groups might be an important factor for the iron transport.}, language = {en} } @misc{Meyer, author = {Meyer, Michael}, title = {Ab Initio Study of Flavonoids}, url = {http://nbn-resolving.de/urn:nbn:de:0297-zib-4110}, number = {SC-99-23}, abstract = {Flavone and the flavylium ion have been studied at Hartree-Fock, M{\o}ller-Plesset and B3LYP hybrid density functional level to determine the structures and barriers to internal rotation. Both molecules have a high perpendicular barrier about the single bond connecting the phenyl ring with the benzopyrone and benzopyrylium ring, respectively. In contrast to biphenyl both molecules have low coplanar barriers. B3LYP overestimates the perpendicular barrier heights compared to other methods. The dependence of the population and orbital energies on the torsion has been investigated and the structures of both flavonoids have been estimated by means of a reaction field model.}, language = {en} }