J. Priestle

发表

Complementarity of hydrophobic properties in ATP‐protein binding: A new criterion to rank docking solutions

E. Jacoby, A. Arseniev, T. Pyrkov, 2006, Proteins.

Three-dimensional structure of the bifunctional enzyme phosphoribosylanthranilate isomerase: indoleglycerolphosphate synthase from Escherichia coli refined at 2.0 A resolution.

M Wilmanns, T. Niermann, M. Wilmanns, 1992, Journal of molecular biology.

Three-dimensional structure of the bifunctional enzyme N-(5'-phosphoribosyl)anthranilate isomerase-indole-3-glycerol-phosphate synthase from Escherichia coli.

T. Jardetzky, M. Grütter, K. Kirschner, 1987, Proceedings of the National Academy of Sciences of the United States of America.

RIBBON: a stereo cartoon drawing program for proteins

J. Priestle, J. P. Priestle, 1988 .

The crystal structures of recombinant glycosylated human renin alone and in complex with a transition state analog inhibitor.

M. Grütter, J. Priestle, M G Grütter, 1991, Journal of structural biology.

A neural net approach to the automated analysis of crystallization trials

J. Priestle, G. Spraggon, S. Lesley, 2002 .

5 – Experimental Techniques and Data Banks

J. Priestle, C. Paris, C. Paris, 1996 .

Improved dihedral-angle restraints for protein structure refinement

J. Priestle, 2003 .

A Lys27‐to‐Glu27 mutation in the human insulin‐like growth factor‐1 prevents disulfide linked dimerization and allows secretion of BiP when expressed in yeast

J. Priestle, B. Chaudhuri, S. B. Helliwell, 1991, FEBS letters.

The structure of murine interleukin-1 beta at 2.8 A resolution.

A. Schmitz, M. Grütter, J. Priestle, 1991, Journal of structural biology.

Changes in interactions in complexes of hirudin derivatives and human α‐thrombin due to different crystal forms

M. Grütter, J. Priestle, J. Rahuel, 1993, Protein science : a publication of the Protein Society.

Refined crystal structures of subtilisin novo in complex with wild-type and two mutant eglins. Comparison with other serine proteinase inhibitor complexes.

K. Wilson, M. Grütter, J. Priestle, 1991, Journal of molecular biology.

Modelling study of protein kinase inhibitors: Binding mode of staurosporine and origin of the selectivity of CGP 52411

Pascal Furet, Peter Traxler, Giorgio Caravatti, 1995, J. Comput. Aided Mol. Des..

The three-dimensional structure of interleukin-1 beta.

M. Grütter, J. Priestle, H. Schär, 1988, Biochemical Society transactions.

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 binding.

J. Priestle, J. van Oostrum, J. Chang, 1992, Biochemistry.

How to Computationally Stack the Deck for Hit-to-Lead Generation: In Silico Molecular Interaction Energy Profiling for de Novo siRNA Guide Strand Surrogate Selection

Marcel J J Blommers, Paulette A Greenidge, Jürg Hunziker, 2019, J. Chem. Inf. Model..

Recombinant hirustasin: Production in yeast, crystallization, and interaction with serine proteases

M. Grütter, G. Fendrich, J. Priestle, 1997, Protein science : a publication of the Protein Society.

The crystal structure of TGF‐β3 and comparison to TGF‐β2: Implications for receptor binding

M. Grütter, P. Mittl, J. Priestle, 1996, Protein science : a publication of the Protein Society.

Structure of Recombinant Human CPP32 in Complex with the Tetrapeptide Acetyl-Asp-Val-Ala-Asp Fluoromethyl Ketone*

M. Grütter, P. Mittl, J. Priestle, 1997, The Journal of Biological Chemistry.

Crystal structure of the thrombin‐hirudin complex: a novel mode of serine protease inhibition.

W. Bode, J. Hofsteenge, W. Bode, 1990, The EMBO journal.

A model for the binding of low molecular weight inhibitors to the active site of thrombin

John P. Priestle, Mark C. Allen, Xiao Ling Fan Cockcroft, 1999, J. Comput. Aided Mol. Des..

Changing the inhibitory specificity and function of the proteinase inhibitor eglin c by site-directed mutagenesis: functional and structural investigation.

Jeffrey W. Peng, S. Hyberts, G. Wagner, 1992, Biochemistry.

Structure of the complex of leech-derived tryptase inhibitor (LDTI) with trypsin and modeling of the LDTI-tryptase system.

J. Priestle, S. Di Marco, 1997, Structure.

A new structural class of serine protease inhibitors revealed by the structure of the hirustasin-kallikrein complex.

M. Grütter, P. Mittl, G. Fendrich, 1997, Structure.

The 1.2 A crystal structure of hirustasin reveals the intrinsic flexibility of a family of highly disulphide-bridged inhibitors.

G Bricogne, G. Sheldrick, G. Bricogne, 1999, Structure.

A mutational analysis of receptor binding sites of interleukin-1β:differences in binding of human interleukin-1β muteins to human and mouse receptors

A. Schmitz, M. Grütter, J. Priestle, 1994 .

Crystallographic refinement of interleukin 1 beta at 2.0 A resolution.

M. Grütter, J. Priestle, H. Schär, 1989, Proceedings of the National Academy of Sciences of the United States of America.

Functional Profiling of Recombinant NS3 Proteases from All Four Serotypes of Dengue Virus Using Tetrapeptide and Octapeptide Substrate Libraries*[boxs]

Jennifer L. Harris, D. Wen, S. Vasudevan, 2005, Journal of Biological Chemistry.

Stereochemical dictionaries for protein structure

J. Priestle, 1994 .

Stereochemical dictionaries for protein structure refinement and model building.

J. Priestle, 1994, Structure.

Crystal structure of the cytokine interleukin‐1 beta.

M. Grütter, J. Priestle, M. Grutter, 1988, The EMBO journal.

Computational analysis of crystallization trials.

Glen Spraggon, Scott A Lesley, Andreas Kreusch, 2002, Acta crystallographica. Section D, Biological crystallography.

A small molecule fusion inhibitor of dengue virus.

P. Shi, J. Priestle, W. Schul, 2009, Antiviral research.

Active site binding loop stabilization in the subtilisin inhibitor eglin c: structural and functional studies on specifically designed mutants in complex with subtilisin and the uncomplexed inhibitor.

M. Grütter, J. Priestle, K. Hipler, 1996, Advances in experimental medicine and biology.

Molecular lipophilicity in protein modeling and drug design.

Edgar Jacoby, Roman G Efremov, John P Priestle, 2007, Current medicinal chemistry.

Restrained Least-Squares Refinement of the Sulfhydryl Protease Papain to 2.0 Angstroms

Christina Thaller, C. Thaller, E. Mehler, 1985 .

The three-dimensional structure of human interleukin-1 beta refined to 2.0 A resolution.

M. Grütter, J. Priestle, H. Schär, 1990, Progress in clinical and biological research.

X‐ray crystal structure of the serine proteinase inhibitor eglin c at 1.95 Å resolution

M. Grütter, J. Priestle, J. Rahuel, 1992, FEBS letters.

Optimisation of the P2 pharmacophore in a series of thrombin inhibitors: ion-dipole interactions with lysine 60G.

M. Grütter, J. Priestle, B. Wathey, 1999, Bioorganic & Medicinal Chemistry Letters.

Improved dihedral-angle restraints for protein structure refinement

J. Priestle, 2003 .