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J P Priestle

Showing results (21-30 of 31) with videos related to

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Journal of Computer-Aided Molecular Design|December 1, 1995
Modelling study of protein kinase inhibitors: binding mode of staurosporine and origin of the selectivity of CGP 52411P Furet, G Caravatti, N Lydon, et al.
Protein Science : a Publication of the Protein Society|July 1, 1996
The crystal structure of TGF-beta 3 and comparison to TGF-beta 2: implications for receptor bindingP R Mittl, J P Priestle, D A Cox, et al.
The EMBO Journal|August 1, 1990
Crystal structure of the thrombin-hirudin complex: a novel mode of serine protease inhibitionM G Grütter, J P Priestle, J Rahuel, et al.
Biochemistry|September 22, 1992
Changing the inhibitory specificity and function of the proteinase inhibitor eglin c by site-directed mutagenesis: functional and structural investigationD W Heinz, S G Hyberts, J W Peng, et al.
Biochemistry|March 24, 1992
Identification of a reactive lysyl residue (Lys103) of recombinant human interleukin-1 beta. Mechanism of its reactivity and implication of its functional role in receptor bindingJ Y Chang, P K Ngai, J P Priestle, et al.
Protein Engineering|May 1, 1994
A mutational analysis of receptor binding sites of interleukin-1 beta: differences in binding of human interleukin-1 beta muteins to human and mouse receptorsM G Grütter, J van Oostrum, J P Priestle, et al.
Protein Science : a Publication of the Protein Society|January 1, 1997
Recombinant hirustasin: production in yeast, crystallization, and interaction with serine proteasesS Di Marco, G Fendrich, R Knecht, et al.
Structure (London, England : 1993)|February 15, 1997
A new structural class of serine protease inhibitors revealed by the structure of the hirustasin-kallikrein complexP R Mittl, S Di Marco, G Fendrich, et al.
Structure (London, England : 1993)|June 16, 1999
The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitorsI Usón, G M Sheldrick, E de La Fortelle, et al.
The Journal of Biological Chemistry|March 7, 1997
Structure of recombinant human CPP32 in complex with the tetrapeptide acetyl-Asp-Val-Ala-Asp fluoromethyl ketoneP R Mittl, S Di Marco, J F Krebs, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Journal of Computer-Aided Molecular Design|December 1, 1995
Modelling study of protein kinase inhibitors: binding mode of staurosporine and origin of the selectivity of CGP 52411P Furet, G Caravatti, N Lydon, et al.
Protein Science : a Publication of the Protein Society|July 1, 1996
The crystal structure of TGF-beta 3 and comparison to TGF-beta 2: implications for receptor bindingP R Mittl, J P Priestle, D A Cox, et al.
The EMBO Journal|August 1, 1990
Crystal structure of the thrombin-hirudin complex: a novel mode of serine protease inhibitionM G Grütter, J P Priestle, J Rahuel, et al.
Biochemistry|September 22, 1992
Changing the inhibitory specificity and function of the proteinase inhibitor eglin c by site-directed mutagenesis: functional and structural investigationD W Heinz, S G Hyberts, J W Peng, et al.
Biochemistry|March 24, 1992
Identification of a reactive lysyl residue (Lys103) of recombinant human interleukin-1 beta. Mechanism of its reactivity and implication of its functional role in receptor bindingJ Y Chang, P K Ngai, J P Priestle, et al.
Protein Engineering|May 1, 1994
A mutational analysis of receptor binding sites of interleukin-1 beta: differences in binding of human interleukin-1 beta muteins to human and mouse receptorsM G Grütter, J van Oostrum, J P Priestle, et al.
Protein Science : a Publication of the Protein Society|January 1, 1997
Recombinant hirustasin: production in yeast, crystallization, and interaction with serine proteasesS Di Marco, G Fendrich, R Knecht, et al.
Structure (London, England : 1993)|February 15, 1997
A new structural class of serine protease inhibitors revealed by the structure of the hirustasin-kallikrein complexP R Mittl, S Di Marco, G Fendrich, et al.
Structure (London, England : 1993)|June 16, 1999
The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitorsI Usón, G M Sheldrick, E de La Fortelle, et al.
The Journal of Biological Chemistry|March 7, 1997
Structure of recombinant human CPP32 in complex with the tetrapeptide acetyl-Asp-Val-Ala-Asp fluoromethyl ketoneP R Mittl, S Di Marco, J F Krebs, et al.
Pageof 4