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Structure of the C-terminally truncated human ProMMP9, a gelatin-binding matrix metalloproteinase

Acta crystallographica. Section D, Biological crystallography., 2002-07, Vol.58 (7), p.1182-1192

2002

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4-Aryl-1,2,3-triazole: A Novel Template for a Reversible Methionine Aminopeptidase 2 Inhibitor, Optimized To Inhibit Angiogenesis in Vivo

Journal of medicinal chemistry, 2005-09, Vol.48 (18), p.5644-5647

2005

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Unique fold and active site in cytomegalovirus protease

Nature (London), 1996-09, Vol.383 (6597), p.275-279

1996

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Highly Potent Inhibitors of Methionine Aminopeptidase-2 Based on a 1,2,4-Triazole Pharmacophore

Journal of medicinal chemistry, 2007-08, Vol.50 (16), p.3777-3785

2007

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Refined structures of β-ketoacyl-acyl carrier protein synthase III

Journal of molecular biology, 2001-03, Vol.307 (1), p.341-356

2001

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Structure Activity Relationships of 5-, 6-, and 7-Methyl-Substituted Azepan-3-one Cathepsin K Inhibitors

Journal of medicinal chemistry, 2006-03, Vol.49 (5), p.1597-1612

2006

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A Historical and Legal Study of Sovereignty in the Canadian North : Terrestrial Sovereignty, 1870-1939

A historical and legal study of sovereignty in the Canadian north, 2014, Vol.no. 17.

1, 2014

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In situ data collection and structure refinement from microcapillary protein crystallization

Journal of applied crystallography, 2005-12, Vol.38 (6), p.900-905

2005

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Structure-Based Design of Lipophilic Quinazoline Inhibitors of Thymidylate Synthase

Journal of medicinal chemistry, 1996-02, Vol.39 (4), p.904-917

1996

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Design of Potent and Selective Human Cathepsin K Inhibitors that Span the Active Site

Proceedings of the National Academy of Sciences - PNAS, 1997-12, Vol.94 (26), p.14249-14254

1997

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Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K

Journal of medicinal chemistry, 2001-03, Vol.44 (5), p.725-736

2001

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The Crystal Structure of Human Procathepsin K

Biochemistry (Easton), 1999-01, Vol.38 (3), p.862-869

1999

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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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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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Active Site Cavity of Herpesvirus Proteases Revealed by the Crystal Structure of Herpes Simplex Virus Protease/Inhibitor Complex

Biochemistry (Easton), 1997-11, Vol.36 (46), p.14023-14029

1997

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Structure-Based Design of Substituted Diphenyl Sulfones and Sulfoxides as Lipophilic Inhibitors of Thymidylate Synthase

Journal of medicinal chemistry, 1997-02, Vol.40 (5), p.677-683

1997

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Crystal Structure of Varicella-Zoster Virus Protease

Proceedings of the National Academy of Sciences - PNAS, 1997-04, Vol.94 (7), p.2874-2879

1997

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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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Use of X-ray Co-crystal Structures and Molecular Modeling To Design Potent and Selective Non-peptide Inhibitors of Cathepsin K

Journal of the American Chemical Society, 1998-09, Vol.120 (35), p.9114-9115

1998

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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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Crystal structure of human osteoclast cathepsin K complex with E-64

Nature structural biology, 1997-02, Vol.4 (2), p.109-111

1997

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Azepanone-Based Inhibitors of Human and Rat Cathepsin K

Journal of medicinal chemistry, 2001-04, Vol.44 (9), p.1380-1395

2001

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Tertiary Structure of Plant RuBisCo: Domains and their Contacts

Science (American Association for the Advancement of Science), 1988-07, Vol.241 (4861), p.71-74

1988

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Crystal structure of beta-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis

The Journal of biological chemistry, 1999-12, Vol.274 (51), p.36465-36471

1999

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Crystal structure of Staphylococcus aureus tyrosyl‐tRNA synthetase in complex with a class of potent and specific inhibitors

Protein science, 2001-10, Vol.10 (10), p.2008-2016

2001

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Structure of the C-terminally truncated human ProMMP9, a gelatin-binding matrix metalloproteinase

4-Aryl-1,2,3-triazole: A Novel Template for a Reversible Methionine Aminopeptidase 2 Inhibitor, Optimized To Inhibit Angiogenesis in Vivo

Unique fold and active site in cytomegalovirus protease

Highly Potent Inhibitors of Methionine Aminopeptidase-2 Based on a 1,2,4-Triazole Pharmacophore

Refined structures of β-ketoacyl-acyl carrier protein synthase III

Structure Activity Relationships of 5-, 6-, and 7-Methyl-Substituted Azepan-3-one Cathepsin K Inhibitors

A Historical and Legal Study of Sovereignty in the Canadian North : Terrestrial Sovereignty, 1870-1939

In situ data collection and structure refinement from microcapillary protein crystallization

Structure-Based Design of Lipophilic Quinazoline Inhibitors of Thymidylate Synthase

Design of Potent and Selective Human Cathepsin K Inhibitors that Span the Active Site

Cyclic Ketone Inhibitors of the Cysteine Protease Cathepsin K

The Crystal Structure of Human Procathepsin 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

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

Active Site Cavity of Herpesvirus Proteases Revealed by the Crystal Structure of Herpes Simplex Virus Protease/Inhibitor Complex

Structure-Based Design of Substituted Diphenyl Sulfones and Sulfoxides as Lipophilic Inhibitors of Thymidylate Synthase

Crystal Structure of Varicella-Zoster Virus Protease

Potent dipeptidylketone inhibitors of the cysteine protease cathepsin K

Use of X-ray Co-crystal Structures and Molecular Modeling To Design Potent and Selective Non-peptide Inhibitors of Cathepsin K

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

Crystal structure of human osteoclast cathepsin K complex with E-64

Azepanone-Based Inhibitors of Human and Rat Cathepsin K

Tertiary Structure of Plant RuBisCo: Domains and their Contacts

Crystal structure of beta-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis

Crystal structure of Staphylococcus aureus tyrosyl‐tRNA synthetase in complex with a class of potent and specific inhibitors

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