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7 results for author:"Ostermann N." in Literature citations

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Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetes.

Sutton J.M., Clark D.E., Dunsdon S.J., Fenton G., Fillmore A., Harris N.V., Higgs C., Hurley C.A., Krintel S.L., MacKenzie R.E. et al.

Bioorg. Med. Chem. Lett. 22:1464-1468(2012) · Mapped (1)

Crystal structure of human BACE2 in complex with a hydroxyethylamine transition-state inhibitor.

Ostermann N., Eder J., Eidhoff U., Zink F., Hassiepen U., Worpenberg S., Maibaum J., Simic O., Hommel U., Gerhartz B.

J. Mol. Biol. 355:249-261(2006) · UniProtKB (1)

Crystal structure of an activation intermediate of cathepsin E.

Ostermann N., Gerhartz B., Worpenberg S., Trappe J., Eder J.

J. Mol. Biol. 342:889-899(2004) · Mapped (2)

Structures of human thymidylate kinase in complex with prodrugs: implications for the structure-based design of novel compounds.

Ostermann N., Segura-Pena D., Meier C., Veit T., Monnerjahn C., Konrad M., Lavie A.

Biochemistry 42:2568-2577(2003) · UniProtKB (1)

Potentiating AZT activation: structures of wild-type and mutant human thymidylate kinase suggest reasons for the mutants' improved kinetics with the HIV prodrug metabolite AZTMP.

Ostermann N., Lavie A., Padiyar S., Brundiers R., Veit T., Reinstein J., Goody R.S., Konrad M., Schlichting I.

J. Mol. Biol. 304:43-53(2000) · Mapped (1)

Insights into the phosphoryltransfer mechanism of human thymidylate kinase gained from crystal structures of enzyme complexes along the reaction coordinate.

Ostermann N., Schlichting I., Brundiers R., Konrad M., Reinstein J., Veit T., Goody R.S., Lavie A.

Structure 8:629-642(2000) · Mapped (1)

Structural basis for efficient phosphorylation of 3'-azidothymidine monophosphate by Escherichia coli thymidylate kinase.

Lavie A., Ostermann N., Brundiers R., Goody R.S., Reinstein J., Konrad M., Schlichting I.

Proc. Natl. Acad. Sci. U.S.A. 95:14045-14050(1998) · UniProtKB (1)

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