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Structural studies of repressors from SorC/DeoR family

Acta crystallographica. Section A, Foundations and advances, 2022-08, Vol.78 (a2), p.e44-e44

2022

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Structure-assisted design of carborane inhibitors of human carbonic anhydrase IX

Acta crystallographica. Section A, Foundations and advances, 2022-08, Vol.78 (a2), p.e41-e41

2022

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The structure and function of Iristatin, a novel immunosuppressive tick salivary cystatin

Cellular and molecular life sciences : CMLS, 2019-05, Vol.76 (10), p.2003-2013

2019

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The effect of outdoor air and indoor human activity on mass concentrations of PM10, PM2.5, and PM1 in a classroom

Environmental research, 2005-10, Vol.99 (2), p.143-149

2005

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Current and Novel Inhibitors of HIV Protease

Viruses, 2009-12, Vol.1 (3), p.1209-1239

2009

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From Nonpeptide toward Noncarbon Protease Inhibitors: Metallacarboranes as Specific and Potent Inhibitors of HIV Protease

Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (43), p.15394-15399

2005

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Structural Basis of HIV-1 and HIV-2 Protease Inhibition by a Monoclonal Antibody

Structure (London), 2001-10, Vol.9 (10), p.887-895

2001

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Molecular Analysis of the HIV-1 Resistance Development: Enzymatic Activities, Crystal Structures, and Thermodynamics of Nelfinavir-resistant HIV Protease Mutants

Journal of molecular biology, 2007-12, Vol.374 (4), p.1005-1016

2007

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Toward the Crystallization of Photosystem II Core Complex from Pisum sativum L

Crystal growth & design, 2010-08, Vol.10 (8), p.3391-3396

2010

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Inhibition of the HIV-1 and HIV-2 proteases by a monoclonal antibody

Protein science, 1999-12, Vol.8 (12), p.2686-2696

1999

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Crystal structure and putative function of small Toprim domain-containing protein from Bacillus stearothermophilus

Proteins, structure, function, and bioinformatics, 2008-02, Vol.70 (2), p.311-319

2008

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Inhibition of HIV protease by monoclonal antibodies

Journal of molecular recognition, 2002-09, Vol.15 (5), p.272-276

2002

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Link between a novel human γD-crystallin allele and a unique cataract phenotype explained by protein crystallography

Human molecular genetics, 2000-07, Vol.9 (12), p.1779-1786

2000

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Development of a Crystallization Protocol for the DbeA 1 Variant of Novel Haloalkane Dehalogenase from Bradyrhizohium elkani USDA94

Crystal growth & design, 2011, Vol.11 (2), p.516-519

2011

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The effect of outdoor air and indoor human activity on mass concentrations of PM sub(1) sub(0), PM sub(2) sub(.) sub(5), and PM sub(1) in a classroom

Environmental research, 2005-10, Vol.99 (2), p.143-149

2005

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Structure-assisted drug discovery: cyclin-dependent kinase 2

Acta crystallographica. Section A, Foundations and advances, 2022-08, Vol.78 (a2), p.e351-e351

2022

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SorC protein family: the structural insight into their DNA recognition

Acta crystallographica. Section A, Foundations and advances, 2022-08, Vol.78 (a2), p.e345-e345

2022

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A Phenylnorstatine Inhibitor Binding to HIV-1 Protease: Geometry, Protonation, and Subsite−Pocket Interactions Analyzed at Atomic Resolution

Journal of medicinal chemistry, 2004-04, Vol.47 (8), p.2030-2036

2004

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Structure-based drug design of selective 5′-nucleotidases inhibitors

Acta crystallographica. Section A, Foundations of crystallography, 2011-08, Vol.67 (a1), p.C227-C227

2011

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CONCENTRATION OF PM1 IN DIFFERENT TYPES OF INDOOR ENVIRONMENT

Journal of aerosol science, 2001-09, Vol.32, p.781-782

2001

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Structural study of Neisseria meningitidis iron-regulated protein FrpD

Acta crystallographica. Section A, Foundations of crystallography, 2011-08, Vol.67 (a1), p.C302-C302

2011

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Potent inhibition of drug-resistant HIV protease variants by monoclonal antibodies

Antiviral research, 2008-06, Vol.78 (3), p.275-277

2008

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Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide

Journal of structural biology, 2005-03, Vol.149 (3), p.332-337

2005

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Inhibitor binding at the protein interface in crystals of a HIV-1 protease complex

Acta crystallographica. Section D, Biological crystallography., 2004-11, Vol.60 (11), p.1943-1948

2004

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Structure of a single-chain Fv fragment of an antibody that inhibits the HIV-1 and HIV-2 proteases

Acta crystallographica. Section D, Biological crystallography., 2003-05, Vol.59 (5), p.955-957

2003

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Structural studies of repressors from SorC/DeoR family

Structure-assisted design of carborane inhibitors of human carbonic anhydrase IX

The structure and function of Iristatin, a novel immunosuppressive tick salivary cystatin

The effect of outdoor air and indoor human activity on mass concentrations of PM10, PM2.5, and PM1 in a classroom

Current and Novel Inhibitors of HIV Protease

From Nonpeptide toward Noncarbon Protease Inhibitors: Metallacarboranes as Specific and Potent Inhibitors of HIV Protease

Structural Basis of HIV-1 and HIV-2 Protease Inhibition by a Monoclonal Antibody

Molecular Analysis of the HIV-1 Resistance Development: Enzymatic Activities, Crystal Structures, and Thermodynamics of Nelfinavir-resistant HIV Protease Mutants

Toward the Crystallization of Photosystem II Core Complex from Pisum sativum L

Inhibition of the HIV-1 and HIV-2 proteases by a monoclonal antibody

Crystal structure and putative function of small Toprim domain-containing protein from Bacillus stearothermophilus

Inhibition of HIV protease by monoclonal antibodies

Link between a novel human γD-crystallin allele and a unique cataract phenotype explained by protein crystallography

Development of a Crystallization Protocol for the DbeA 1 Variant of Novel Haloalkane Dehalogenase from Bradyrhizohium elkani USDA94

The effect of outdoor air and indoor human activity on mass concentrations of PM sub(1) sub(0), PM sub(2) sub(.) sub(5), and PM sub(1) in a classroom

Structure-assisted drug discovery: cyclin-dependent kinase 2

SorC protein family: the structural insight into their DNA recognition

A Phenylnorstatine Inhibitor Binding to HIV-1 Protease: Geometry, Protonation, and Subsite−Pocket Interactions Analyzed at Atomic Resolution

Structure-based drug design of selective 5′-nucleotidases inhibitors

CONCENTRATION OF PM1 IN DIFFERENT TYPES OF INDOOR ENVIRONMENT

Structural study of Neisseria meningitidis iron-regulated protein FrpD

Potent inhibition of drug-resistant HIV protease variants by monoclonal antibodies

Crystal structure of a cross-reaction complex between an anti-HIV-1 protease antibody and an HIV-2 protease peptide

Inhibitor binding at the protein interface in crystals of a HIV-1 protease complex

Structure of a single-chain Fv fragment of an antibody that inhibits the HIV-1 and HIV-2 proteases

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