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Nature|January 7, 1993
Solution structure of the cyclosporin A/cyclophilin complex by NMRY Thériault, T M Logan, R Meadows, et al.Journal of Medicinal Chemistry|February 1, 1988
Renin inhibitors. Design and synthesis of a new class of conformationally restricted analogues of angiotensinogenH L Sham, G Bolis, H H Stein, et al.Journal of Medicinal Chemistry|June 26, 1992
NMR studies of an FK-506 analog, [U-13C]ascomycin, bound to FK-506-binding proteinA M Petros, G Gemmecker, P Neri, et al.Nature|January 5, 2001
Structural basis for binding of Smac/DIABLO to the XIAP BIR3 domainZ Liu, C Sun, E T Olejniczak, et al.Proceedings of the National Academy of Sciences of the United States of America|March 15, 2001
Solution structure of the antiapoptotic protein bcl-2A M Petros, A Medek, D G Nettesheim, et al.Nature Structural Biology|April 1, 1996
Structural basis for IL-4 receptor phosphopeptide recognition by the IRS-1 PTB domainM M Zhou, B Huang, E T Olejniczak, et al.Journal of Molecular Biology|August 9, 2001
Solution structure and function of a conserved protein SP14.3 encoded by an essential Streptococcus pneumoniae geneL Yu, A H Gunasekera, J Mack, et al.Journal of Medicinal Chemistry|November 2, 1999
Retention of immunosuppressant activity in an ascomycin analogue lacking a hydrogen-bonding interaction with FKBP12P E Wiedeman, S W Fesik, A M Petros, et al.Proceedings of the National Academy of Sciences of the United States of America|August 15, 1995
Solution structure of the Shc SH2 domain complexed with a tyrosine-phosphorylated peptide from the T-cell receptorM M Zhou, R P Meadows, T M Logan, et al.Oncogene|October 26, 2005
RNAi-based screening of the human kinome identifies Akt-cooperating kinases: a new approach to designing efficacious multitargeted kinase inhibitorsS Morgan-Lappe, K W Woods, Q Li, et al.Pageof 186