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The EMBO Journal|March 15, 1996
The nature of inhibition of DNA gyrase by the coumarins and the cyclothialidines revealed by X-ray crystallographyR J Lewis, O M Singh, C V Smith, et al.Journal of Molecular Biology|November 5, 1989
Crystallization and preliminary X-ray analysis of porcine synovial collagenaseL F Lloyd, T Skarzyński, A J Wonacott, et al.Bioorganic & Medicinal Chemistry Letters|March 27, 2001
Sialidase inhibitors related to zanamivir. Further SAR studies of 4-amino-4H-pyran-2-carboxylic acid-6-propylamidesP G Wyatt, B A Coomber, D N Evans, et al.The Journal of Biological Chemistry|December 23, 1999
X-ray crystal structure of human dopamine sulfotransferase, SULT1A3. Molecular modeling and quantitative structure-activity relationship analysis demonstrate a molecular basis for sulfotransferase substrate specificityR Dajani, A Cleasby, M Neu, et al.Journal of Medicinal Chemistry|April 4, 1998
Dihydropyrancarboxamides related to zanamivir: a new series of inhibitors of influenza virus sialidases. 2. Crystallographic and molecular modeling study of complexes of 4-amino-4H-pyran-6-carboxamides and sialidase from influenza virus types A and BN R Taylor, A Cleasby, O Singh, et al.Proteins|May 1, 1997
The high-resolution crystal structure of a 24-kDa gyrase B fragment from E. coli complexed with one of the most potent coumarin inhibitors, clorobiocinF T Tsai, O M Singh, T Skarzynski, et al.Biochemistry|June 6, 1998
Novel natural product 5,5-trans-lactone inhibitors of human alpha-thrombin: mechanism of action and structural studiesM P Weir, S S Bethell, A Cleasby, et al.Pageof 2