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C A Pargellis

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The Journal of Biological Chemistry|November 22, 1996
Identification and characterization of the N-ethylmaleimide-sensitive site in lambda-integraseR S Tirumalai, C A Pargellis, A Landy
Archives of Biochemistry and Biophysics|April 15, 1996
Kinetic characterization of human immunodeficiency virus type 1 protease: determination of inhibitor rate constants during dynamic monomer-dimer interconversionM M Morelock, E T Graham, D Erdman, et al.
The Journal of Biological Chemistry|June 5, 1988
Suicide recombination substrates yield covalent lambda integrase-DNA complexes and lead to identification of the active site tyrosineC A Pargellis, S E Nunes-Düby, L M de Vargas, et al.
Journal of Medicinal Chemistry|May 12, 1995
Time-resolved ligand exchange reactions: kinetic models for competitive inhibitors with recombinant human reninM M Morelock, C A Pargellis, E T Graham, et al.
Journal of Enzyme Inhibition|January 1, 1997
Inhibition of dipeptidyl peptidase IV (CD26) by peptide boronic acid dipeptidesC A Pargellis, S J Campbell, S Pav, et al.
Cell|September 23, 1988
Autonomous DNA binding domains of lambda integrase recognize two different sequence familiesL Moitoso de Vargas, C A Pargellis, N M Hasan, et al.
Nature Structural Biology|April 1, 1997
A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocketL Tong, S Pav, D M White, et al.
Biochemistry|October 18, 1994
Determination of kinetic rate constants for the binding of inhibitors to HIV-1 protease and for the association and dissociation of active homodimerC A Pargellis, M M Morelock, E T Graham, et al.
Protein Science : a Publication of the Protein Society|January 1, 1997
Crystallization and preliminary crystallographic analysis of recombinant human P38 MAP kinaseS Pav, D M White, S Rogers, et al.
Biochemical Pharmacology|December 13, 1996
Effect of deoxycoformycin and Val-boroPro on the associated catalytic activities of lymphocyte CD26 and ecto-adenosine deaminaseD D Jeanfavre, J R Woska, C A Pargellis, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
The Journal of Biological Chemistry|November 22, 1996
Identification and characterization of the N-ethylmaleimide-sensitive site in lambda-integraseR S Tirumalai, C A Pargellis, A Landy
Archives of Biochemistry and Biophysics|April 15, 1996
Kinetic characterization of human immunodeficiency virus type 1 protease: determination of inhibitor rate constants during dynamic monomer-dimer interconversionM M Morelock, E T Graham, D Erdman, et al.
The Journal of Biological Chemistry|June 5, 1988
Suicide recombination substrates yield covalent lambda integrase-DNA complexes and lead to identification of the active site tyrosineC A Pargellis, S E Nunes-Düby, L M de Vargas, et al.
Journal of Medicinal Chemistry|May 12, 1995
Time-resolved ligand exchange reactions: kinetic models for competitive inhibitors with recombinant human reninM M Morelock, C A Pargellis, E T Graham, et al.
Journal of Enzyme Inhibition|January 1, 1997
Inhibition of dipeptidyl peptidase IV (CD26) by peptide boronic acid dipeptidesC A Pargellis, S J Campbell, S Pav, et al.
Cell|September 23, 1988
Autonomous DNA binding domains of lambda integrase recognize two different sequence familiesL Moitoso de Vargas, C A Pargellis, N M Hasan, et al.
Nature Structural Biology|April 1, 1997
A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocketL Tong, S Pav, D M White, et al.
Biochemistry|October 18, 1994
Determination of kinetic rate constants for the binding of inhibitors to HIV-1 protease and for the association and dissociation of active homodimerC A Pargellis, M M Morelock, E T Graham, et al.
Protein Science : a Publication of the Protein Society|January 1, 1997
Crystallization and preliminary crystallographic analysis of recombinant human P38 MAP kinaseS Pav, D M White, S Rogers, et al.
Biochemical Pharmacology|December 13, 1996
Effect of deoxycoformycin and Val-boroPro on the associated catalytic activities of lymphocyte CD26 and ecto-adenosine deaminaseD D Jeanfavre, J R Woska, C A Pargellis, et al.
Pageof 1