Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Peter Reinemer"'
Autor:
Harald Mückter, Robin Lüling, Markus Siegert, Harald John, Horst Thiermann, Tanja Popp, Peter Reinemer, Dirk Steinritz, Thomas Gudermann
Publikováno v:
Archives of Toxicology
Creatine kinase (CK) catalyzes the formation of phosphocreatine from adenosine triphosphate (ATP) and creatine. The highly reactive free cysteine residue in the active site of the enzyme (Cys283) is considered essential for the enzymatic activity. In
Autor:
Stefan Steinbacher, Michel Weïwer, Surya A. Reis, Peter Müller, Peter Reinemer, Adrian Schomburg, Jennifer P. Gale, Daniel M. Fass, Stephen J. Haggarty, Krista M. Hennig, Edward B. Holson, Yan-Ling Zhang, Méryl Thomas, Florence F. Wagner, Stewart L. Fisher, Arthur J. Campbell, Wen-Ning Zhao, Martin R. Jefson
Publikováno v:
Bioorganic & Medicinal Chemistry. 24:4008-4015
The structure-activity and structure-kinetic relationships of a series of novel and selective ortho-aminoanilide inhibitors of histone deacetylases (HDACs) 1 and 2 are described. Different kinetic and thermodynamic selectivity profiles were obtained
Autor:
F. X. Gomis-Rüth, Walter Stöcker, Ulrich Baumann, Frank Grams, Wolfram Bode, David B. McKay, Peter Reinemer
Publikováno v:
Protein Science. 4:823-840
The three-dimensional structures of the zinc endopeptidases human neutrophil collagenase, adamalysin II from rattle snake venom, alkaline proteinase from Pseudomonas aeruginosa, and astacin from crayfish are topologically similar, with respect to a f
Autor:
Wolfram Bode, Peter Reinemer, Luis Moroder, Sergio A. Cadamuro, Peter Goettig, Holger Steuber, Marion G. Götz, Michael Willem, Christian Renner, Tanja Kohler, Anja Jestel, Alessandra Barazza
Publikováno v:
ChemBioChem. 8:2078-2091
Minimal sequence requirements for binding of substrate-derived statine peptides to the aspartyl enzyme were established on the basis of the X-ray cocrystal structure of the hydroxyethylene-octapeptide OM00-3 in complexation with BACE-1. With this inf
Autor:
Marc Stadler, Kevin B. Bacon, Peter Reinemer, Hartwig Müller, Florian Gantner, Hans-Volker Tichy, Jens Bitzer, Jordi Benet-Buchholz, Anke Mayer-Bartschmid
Publikováno v:
Journal of Natural Products. 70:246-252
The cinnabaramides A-G (1-7) were isolated from a terrestrial strain of Streptomyces as potent and selective inhibitors of the human 20S proteasome. Their chemical and biological properties resemble those of salinosporamide A, a recently identified l
Publikováno v:
PROTEOMICS. 6:2947-2958
Authentic biomarkers, distilling the essence of a complex, functionally significant process in a mammalian system into a precise, physicochemical measurement have been implicated as a tool of increasing importance for drug discovery and development.
Publikováno v:
Journal of Molecular Biology. 358:1328-1340
DNA topoisomerases are a family of enzymes altering the topology of DNA by concerted breakage and rejoining of the phosphodiester backbone of DNA. Bacterial and archeal type IA topoisomerases, including topoisomerase I, topoisomerase III, and reverse
Autor:
Alexander Straub, Thomas Lampe, Josef Pernerstorfer, Jens Pohlmann, Karl-Heinz Schlemmer, Elisabeth Perzborn, Susanne Roehrig, Peter Reinemer
Publikováno v:
Journal of Medicinal Chemistry. 48:5900-5908
Despite recent progress in antithrombotic therapy, there is still an unmet medical need for safe and orally available anticoagulants. The coagulation enzyme Factor Xa (FXa) is a particularly promising target, and recent efforts in this field have foc
Publikováno v:
Angewandte Chemie. 39:2834-2846
Organic synthesis of hormone derivatives is an established route to yield pharmacologically active agents. Until recently this has only been feasible for small organic compounds, but nowadays it is also possible to produce antagonists for larger prot
Publikováno v:
Angewandte Chemie. 112:2954-2966