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Impact of Chemical Cross-Linking on Protein Structure and Function

Analytical chemistry (Washington), 2018-01, Vol.90 (2), p.1104-1113

2018

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Anaerobic peroxisomes in Entamoeba histolytica metabolize myo-inositol

PLoS pathogens, 2021-11, Vol.17 (11), p.e1010041-e1010041

2021

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Oligomeric Architecture of Mouse Activating Nkrp1 Receptors on Living Cells

International journal of molecular sciences, 2019-04, Vol.20 (8), p.1884

2019

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Solution structure of the lymphocyte receptor Nkrp1a reveals a distinct conformation of the long loop region as compared to in the crystal structure

Proteins, structure, function, and bioinformatics, 2016-09, Vol.84 (9), p.1304-1311

2016

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Nkrp1 family, from lectins to protein interacting molecules

Molecules (Basel, Switzerland), 2015-02, Vol.20 (2), p.3463-3478

2015

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Structural Model of Lymphocyte Receptor NKR-P1C Revealed by Mass Spectrometry and Molecular Modeling

Analytical chemistry (Washington), 2013-02, Vol.85 (3), p.1597-1604

2013

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Re-evaluation of binding properties of recombinant lymphocyte receptors NKR-P1A and CD69 to chemically synthesized glycans and peptides

International journal of molecular sciences, 2014-01, Vol.15 (1), p.1271-1283

2014

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Re-evaluation of the involvement of NK cells and C-type lectin-like NK receptors in modulation of immune responses by multivalent GlcNAc-terminated oligosaccharides

Immunology letters, 2013-11, Vol.156 (1), p.110-117

2013

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Retraction of Cooperation between Subunits Is Essential for High-Affinity Binding of N‑Acetyl‑d‑hexosamines to Dimeric Soluble and Dimeric Cellular Forms of Human CD69

Biochemistry (Easton), 2014-05, Vol.53 (17), p.2864-2864

2014

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Molecular architecture of mouse activating NKR-P1 receptors

Journal of structural biology, 2011-09, Vol.175 (3), p.434-441

2011

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Structural analysis of natural killer cell receptor protein 1 (NKR-P1) extracellular domains suggests a conserved long loop region involved in ligand specificity

Journal of molecular modeling, 2011-06, Vol.17 (6), p.1353-1370

2011

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Cooperation between Subunits Is Essential for High-Affinity Binding of N-Acetyl-d-hexosamines to Dimeric Soluble and Dimeric Cellular Forms of Human CD69

Biochemistry (Easton), 2010-05, Vol.49 (19), p.4060-4067

2010

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High-level expression of soluble form of mouse natural killer cell receptor NKR-P1C(B6) in Escherichia coli

Protein expression and purification, 2011-06, Vol.77 (2), p.178-184

2011

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Solution structure of the lymphocyte receptor Nkrp1a reveals a distinct conformation of the long loop region as compared to in the crystal structure: Solution Structure of the Receptor Nkrp1a

Proteins, structure, function, and bioinformatics, 2016-09, Vol.84 (9), p.1304-1311

2016

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Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Nature communications, 2018-08, Vol.9 (1), p.3137-13, Article 3137

2018

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Structure of the H107R variant of the extracellular domain of mouse NKR-P1A at 2.3 Å resolution

Acta crystallographica. Section F, Structural biology and crystallization communications, 2011-12, Vol.67 (12), p.1519-1523

2011

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Primary and secondary functions of HLA-E are determined by stability and conformation of the peptide-bound complexes

Cell reports (Cambridge), 2022-06, Vol.39 (11), p.110959-110959, Article 110959

2022

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Diversity of oligomerization in Drosophila semaphorins suggests a mechanism of functional fine-tuning

Nature communications, 2019-08, Vol.10 (1), p.3691-12, Article 3691

2019

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Cell guidance ligands, receptors and complexes – orchestrating signalling in time and space

Current opinion in structural biology, 2020-04, Vol.61, p.79-85

2020

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Synthetic N-Acetyl-d-glucosamine Based Fully Branched Tetrasaccharide, a Mimetic of the Endogenous Ligand for CD69, Activates CD69+ Killer Lymphocytes upon Dimerization via a Hydrophilic Flexible Linker

Journal of medicinal chemistry, 2010-05, Vol.53 (10), p.4050-4065

2010

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Author Correction: Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Nature communications, 2018-11, Vol.9 (1), p.4833-1, Article 4833

2018

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Mouse and human antibodies bind HLA-E-leader peptide complexes and enhance NK cell cytotoxicity

Communications biology, 2022-03, Vol.5 (1), p.271-271, Article 271

2022

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Domain swapping in structure of mNKR-P1A: unique feature with unknown function

Acta crystallographica. Section A, Foundations and advances, 2014-08, Vol.70 (a1), p.C249-C249

2014

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The guidance receptor plexin D1 is a mechanosensor in endothelial cells

Nature (London), 2020-02, Vol.578 (7794), p.290-295

2020

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Impact of Chemical Cross-Linking on Protein Structure and Function

Anaerobic peroxisomes in Entamoeba histolytica metabolize myo-inositol

Oligomeric Architecture of Mouse Activating Nkrp1 Receptors on Living Cells

Solution structure of the lymphocyte receptor Nkrp1a reveals a distinct conformation of the long loop region as compared to in the crystal structure

Nkrp1 family, from lectins to protein interacting molecules

Structural Model of Lymphocyte Receptor NKR-P1C Revealed by Mass Spectrometry and Molecular Modeling

Re-evaluation of binding properties of recombinant lymphocyte receptors NKR-P1A and CD69 to chemically synthesized glycans and peptides

Re-evaluation of the involvement of NK cells and C-type lectin-like NK receptors in modulation of immune responses by multivalent GlcNAc-terminated oligosaccharides

Retraction of Cooperation between Subunits Is Essential for High-Affinity Binding of N‑Acetyl‑d‑hexosamines to Dimeric Soluble and Dimeric Cellular Forms of Human CD69

Retraction: Synthetic N‑Acetyl‑d‑glucosamine Based Fully Branched Tetrasaccharide, a Mimetic of the Endogenous Ligand for CD69, Activates CD69+ Killer Lymphocytes upon Dimerization via a Hydrophilic Flexible Linker

Molecular architecture of mouse activating NKR-P1 receptors

Structural analysis of natural killer cell receptor protein 1 (NKR-P1) extracellular domains suggests a conserved long loop region involved in ligand specificity

Cooperation between Subunits Is Essential for High-Affinity Binding of N-Acetyl-d-hexosamines to Dimeric Soluble and Dimeric Cellular Forms of Human CD69

High-level expression of soluble form of mouse natural killer cell receptor NKR-P1C(B6) in Escherichia coli

Solution structure of the lymphocyte receptor Nkrp1a reveals a distinct conformation of the long loop region as compared to in the crystal structure: Solution Structure of the Receptor Nkrp1a

Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Structure of the H107R variant of the extracellular domain of mouse NKR-P1A at 2.3 Å resolution

Primary and secondary functions of HLA-E are determined by stability and conformation of the peptide-bound complexes

Diversity of oligomerization in Drosophila semaphorins suggests a mechanism of functional fine-tuning

Cell guidance ligands, receptors and complexes – orchestrating signalling in time and space

Synthetic N-Acetyl-d-glucosamine Based Fully Branched Tetrasaccharide, a Mimetic of the Endogenous Ligand for CD69, Activates CD69+ Killer Lymphocytes upon Dimerization via a Hydrophilic Flexible Linker

Author Correction: Pathogen-derived HLA-E bound epitopes reveal broad primary anchor pocket tolerability and conformationally malleable peptide binding

Mouse and human antibodies bind HLA-E-leader peptide complexes and enhance NK cell cytotoxicity

Domain swapping in structure of mNKR-P1A: unique feature with unknown function

The guidance receptor plexin D1 is a mechanosensor in endothelial cells

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