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Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identification

The Journal of biological chemistry, 1996-05, Vol.271 (21), p.12517-12524

1996

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Peptide Aldehyde Inhibitors of Cathepsin K Inhibit Bone Resorption Both In Vitro and In Vivo

Journal of bone and mineral research, 1997-09, Vol.12 (9), p.1396-1406

1997

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Inhibition of Human Immunodeficiency Virus 1 Protease in vitro: Rational Design of Substrate Analogue Inhibitors

Proceedings of the National Academy of Sciences - PNAS, 1989-12, Vol.86 (24), p.9752-9756

1989

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Authenticity and Wooden Architecture Preservation in Asia - a Chinese perspective

Tomaszek, Tomasz

1, 2023

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Hydroxyethylene isostere inhibitors of human immunodeficiency virus-1 protease: structure-activity analysis using enzyme kinetics, x-ray crystallography, and infected T-cell assays

Biochemistry (Easton), 1992-07, Vol.31 (29), p.6646-6659

1992

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Conformationally Constrained 1,3-Diamino Ketones: A Series of Potent Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 1998-09, Vol.41 (19), p.3563-3567

1998

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Use of Papain as a Model for the Structure-Based Design of Cathepsin K Inhibitors: Crystal Structures of Two Papain−Inhibitor Complexes Demonstrate Binding to S‘-Subsites

Journal of medicinal chemistry, 1998-11, Vol.41 (23), p.4567-4576

1998

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Development and Characterization of a Human In Vitro Resorption Assay: Demonstration of Utility Using Novel Antiresorptive Agents

Journal of bone and mineral research, 1999-09, Vol.14 (9), p.1562-1569

1999

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Structure-Based Design of Cathepsin K Inhibitors Containing a Benzyloxy-Substituted Benzoyl Peptidomimetic

Journal of medicinal chemistry, 1998-10, Vol.41 (21), p.3923-3927

1998

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A symmetric inhibitor binds HIV-1 protease asymmetrically

Biochemistry (Easton), 1993, Vol.32 (3), p.937-947

1993

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Authenticity in preservation of Historical Wooden Architecture - Problems and Challenges: Case Studies from the American South

Tomaszek, Tomasz

1st edition, 2020

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A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of .gamma.-turn mimetics into a model substrate

Journal of medicinal chemistry, 1993-08, Vol.36 (16), p.2321-2331

1993

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Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues

Nature (London), 1990-01, Vol.343 (6253), p.90-92

1990

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Rational Design, Synthesis, and Crystallographic Analysis of a Hydroxyethylene-Based HIV-1 Protease Inhibitor Containing a Heterocyclic P1'-P2' Amide Bond Isostere

Journal of medicinal chemistry, 1994-09, Vol.37 (19), p.3100-3107

1994

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Proteolysis of an active site peptide of lactate dehydrogenase by human immunodeficiency virus type 1 protease

Biochemistry (Easton), 1992-10, Vol.31 (42), p.10153-10168

1992

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Purification and biochemical characterization of recombinant simian immunodeficiency virus protease and comparison to human immunodeficiency virus type 1 protease

Biochemistry (Easton), 1991-08, Vol.30 (34), p.8424-8434

1991

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Design and synthesis of diaminopyrrolidinone inhibitors of human osteoclast cathepsin K

Bioorganic & medicinal chemistry letters, 1999-07, Vol.9 (14), p.1907-1910

1999

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Chromophoric peptide substrates for the spectrophotometric assay of HIV-1 protease

Biochemical and biophysical research communications, 1990-04, Vol.168 (1), p.274-280

1990

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Benzodioxocin-3-ones and N-acyl-3-amino-3-buten-2-ones: novel classes of cathepsin K cysteine protease inhibitors

The journal of peptide research, 2004-03, Vol.63 (3), p.265-269

2004

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Hydrolysis of adenyl-5-yl imidodiphosphate by beef heart mitochondrial ATPase

The Journal of biological chemistry, 1986-02, Vol.261 (5), p.2264-2269

1986

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Structure and Design of Potent and Selective Cathepsin K Inhibitors

Journal of the American Chemical Society, 1997-11, Vol.119 (46), p.11351-11352

1997

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Potent and Selective Cathepsin L Inhibitors Do Not Inhibit Human Osteoclast Resorption in Vitro

The Journal of biological chemistry, 2001-04, Vol.276 (15), p.11507-11511

2001

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Mechanism of Inhibition of Cathepsin K by Potent, Selective 1,5-Diacylcarbohydrazides: A New Class of Mechanism-Based Inhibitors of Thiol Proteases

Biochemistry (Easton), 1999-11, Vol.38 (48), p.15893-15902

1999

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Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K

Bioorganic & medicinal chemistry, 1999-04, Vol.7 (4), p.581-588

1999

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Progress in Environmental Engineering: Water, Wastewater Treatment and Environmental Protection Issues

1, 2015

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Proteolytic activity of human osteoclast cathepsin K. Expression, purification, activation, and substrate identification

Peptide Aldehyde Inhibitors of Cathepsin K Inhibit Bone Resorption Both In Vitro and In Vivo

Inhibition of Human Immunodeficiency Virus 1 Protease in vitro: Rational Design of Substrate Analogue Inhibitors

Authenticity and Wooden Architecture Preservation in Asia - a Chinese perspective

Hydroxyethylene isostere inhibitors of human immunodeficiency virus-1 protease: structure-activity analysis using enzyme kinetics, x-ray crystallography, and infected T-cell assays

Conformationally Constrained 1,3-Diamino Ketones: A Series of Potent Inhibitors of the Cysteine Protease Cathepsin K

Use of Papain as a Model for the Structure-Based Design of Cathepsin K Inhibitors: Crystal Structures of Two Papain−Inhibitor Complexes Demonstrate Binding to S‘-Subsites

Development and Characterization of a Human In Vitro Resorption Assay: Demonstration of Utility Using Novel Antiresorptive Agents

Structure-Based Design of Cathepsin K Inhibitors Containing a Benzyloxy-Substituted Benzoyl Peptidomimetic

A symmetric inhibitor binds HIV-1 protease asymmetrically

Authenticity in preservation of Historical Wooden Architecture - Problems and Challenges: Case Studies from the American South

A novel constrained reduced-amide inhibitor of HIV-1 protease derived from the sequential incorporation of .gamma.-turn mimetics into a model substrate

Inhibition of HIV-1 protease in infected T-lymphocytes by synthetic peptide analogues

Rational Design, Synthesis, and Crystallographic Analysis of a Hydroxyethylene-Based HIV-1 Protease Inhibitor Containing a Heterocyclic P1'-P2' Amide Bond Isostere

Proteolysis of an active site peptide of lactate dehydrogenase by human immunodeficiency virus type 1 protease

Purification and biochemical characterization of recombinant simian immunodeficiency virus protease and comparison to human immunodeficiency virus type 1 protease

Design and synthesis of diaminopyrrolidinone inhibitors of human osteoclast cathepsin K

Chromophoric peptide substrates for the spectrophotometric assay of HIV-1 protease

Benzodioxocin-3-ones and N-acyl-3-amino-3-buten-2-ones: novel classes of cathepsin K cysteine protease inhibitors

Hydrolysis of adenyl-5-yl imidodiphosphate by beef heart mitochondrial ATPase

Structure and Design of Potent and Selective Cathepsin K Inhibitors

Potent and Selective Cathepsin L Inhibitors Do Not Inhibit Human Osteoclast Resorption in Vitro

Mechanism of Inhibition of Cathepsin K by Potent, Selective 1,5-Diacylcarbohydrazides: A New Class of Mechanism-Based Inhibitors of Thiol Proteases

Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K

Progress in Environmental Engineering: Water, Wastewater Treatment and Environmental Protection Issues

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