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Identification by Site-directed Mutagenesis of Residues Involved in Ligand Recognition and Activation of the Human A3 Adenosine Receptor

The Journal of biological chemistry, 2002-05, Vol.277 (21), p.19056-19063

2002

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Crystal Structures of Aged Phosphonylated Acetylcholinesterase: Nerve Agent Reaction Products at the Atomic Level

Biochemistry (Easton), 1999-06, Vol.38 (22), p.7032-7039

1999

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Functional Characteristics of the Oxyanion Hole in Human Acetylcholinesterase

The Journal of biological chemistry, 1998-07, Vol.273 (31), p.19509-19517

1998

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Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A2A Adenosine Receptor Crystallographic Structure

Journal of medicinal chemistry, 2009-05, Vol.52 (10), p.3284-3292

2009

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Evaluation of homology modeling of G-protein-coupled receptors in light of the A(2A) adenosine receptor crystallographic structure

Journal of medicinal chemistry, 2009-05, Vol.52 (10), p.3284

2009

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Constitutive Activation of A3 Adenosine Receptors by Site-Directed Mutagenesis

Biochemical and biophysical research communications, 2001-06, Vol.284 (3), p.596-601

2001

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The Architecture of Human Acetylcholinesterase Active Center Probed by Interactions with Selected Organophosphate Inhibitors

The Journal of biological chemistry, 1996-05, Vol.271 (20), p.11953-11962

1996

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Contribution of Aromatic Moieties of Tyrosine 133 and of the Anionic Subsite Tryptophan 86 to Catalytic Efficiency and Allosteric Modulation of Acetylcholinesterase (∗)

The Journal of biological chemistry, 1995-02, Vol.270 (5), p.2082-2091

1995

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Ligand-G Protein Allosteric Communication through Internal Waters in GPCR Complexes

Biophysical journal, 2015-01, Vol.108 (2), p.363a-364a

2015

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The Role of Internal Water in GPCR Complexes

Biophysical journal, 2013-01, Vol.104 (2), p.41a-41a

2013

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Carbocation-Mediated Processes in Biocatalysts. Contribution of Aromatic Moieties

Journal of the American Chemical Society, 1997-04, Vol.119 (13), p.3157-3158

1997

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Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions

Biochemical journal, 2009-01, Vol.417 (1), p.213-222

2009

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A preliminary comparison of structural models for catalytic intermediates of acetylcholinesterase

Chemico-biological interactions, 1999-05, Vol.119-120, p.43-52

1999

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Structural determinants of A(3) adenosine receptor activation: nucleoside ligands at the agonist/antagonist boundary

Journal of medicinal chemistry, 2002-09, Vol.45 (20), p.4471

2002

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Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A 2A Adenosine Receptor Crystallographic Structure

Journal of medicinal chemistry, 2009-05, Vol.52 (10), p.3284-3292

2009

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Structural Determinants of A3 Adenosine Receptor Activation: Nucleoside Ligands at the Agonist/Antagonist Boundary

Journal of medicinal chemistry, 2002-09, Vol.45 (20), p.4471-4484

2002

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Direct determination of the chemical composition of acetylcholinesterase phosphonylation products utilizing electrospray-ionization mass spectrometry

FEBS letters, 1997-05, Vol.407 (3), p.347-352

1997

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Function-specific blockage of M1 and M3 muscarinic acetylcholine receptors by VX and echothiophate

Brain research, 2006-04, Vol.1085 (1), p.102-110

2006

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Flexibility versus “rigidity” of the functional architecture of AChE active center

Chemico-biological interactions, 2008-09, Vol.175 (1), p.166-172

2008

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Efficacy and Safety of Intravenous Immunoglobulin in Patients with Metastatic Melanoma

Annals of the New York Academy of Sciences, 2007-09, Vol.1110 (1), p.305-314

2007

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Function-specific blockage of M(1) and M(3) muscarinic acetylcholine receptors by VX and echothiophate

Brain research, 2006-04, Vol.1085 (1), p.102

2006

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Homology model-assisted elucidation of binding sites in GPCRs

Methods in molecular biology (Clifton, N.J.), 2012, Vol.914, p.179

2012

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Acyclic and Cyclopropyl Analogues of Adenosine Bisphosphate Antagonists of the P2Y1 Receptor: Structure−Activity Relationships and Receptor Docking

Journal of medicinal chemistry, 2001-09, Vol.44 (19), p.3092-3108

2001

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Aging of phosphylated human acetylcholinesterase: catalytic processes mediated by aromatic and polar residues of the active centre

Biochemical journal, 1996-09, Vol.318 ( Pt 3) (3), p.833-840

1996

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Neoceptor Concept Based on Molecular Complementarity in GPCRs: A Mutant Adenosine A3 Receptor with Selectively Enhanced Affinity for Amine-Modified Nucleosides

Journal of medicinal chemistry, 2001-11, Vol.44 (24), p.4125-4136

2001

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Identification by Site-directed Mutagenesis of Residues Involved in Ligand Recognition and Activation of the Human A3 Adenosine Receptor

Crystal Structures of Aged Phosphonylated Acetylcholinesterase: Nerve Agent Reaction Products at the Atomic Level

Functional Characteristics of the Oxyanion Hole in Human Acetylcholinesterase

Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A2A Adenosine Receptor Crystallographic Structure

Evaluation of homology modeling of G-protein-coupled receptors in light of the A(2A) adenosine receptor crystallographic structure

Constitutive Activation of A3 Adenosine Receptors by Site-Directed Mutagenesis

The Architecture of Human Acetylcholinesterase Active Center Probed by Interactions with Selected Organophosphate Inhibitors

Contribution of Aromatic Moieties of Tyrosine 133 and of the Anionic Subsite Tryptophan 86 to Catalytic Efficiency and Allosteric Modulation of Acetylcholinesterase (∗)

Ligand-G Protein Allosteric Communication through Internal Waters in GPCR Complexes

The Role of Internal Water in GPCR Complexes

Carbocation-Mediated Processes in Biocatalysts. Contribution of Aromatic Moieties

Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions

A preliminary comparison of structural models for catalytic intermediates of acetylcholinesterase

Structural determinants of A(3) adenosine receptor activation: nucleoside ligands at the agonist/antagonist boundary

Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A 2A Adenosine Receptor Crystallographic Structure

Structural Determinants of A3 Adenosine Receptor Activation: Nucleoside Ligands at the Agonist/Antagonist Boundary

Direct determination of the chemical composition of acetylcholinesterase phosphonylation products utilizing electrospray-ionization mass spectrometry

Function-specific blockage of M1 and M3 muscarinic acetylcholine receptors by VX and echothiophate

Flexibility versus “rigidity” of the functional architecture of AChE active center

Efficacy and Safety of Intravenous Immunoglobulin in Patients with Metastatic Melanoma

Function-specific blockage of M(1) and M(3) muscarinic acetylcholine receptors by VX and echothiophate

Homology model-assisted elucidation of binding sites in GPCRs

Acyclic and Cyclopropyl Analogues of Adenosine Bisphosphate Antagonists of the P2Y1 Receptor: Structure−Activity Relationships and Receptor Docking

Aging of phosphylated human acetylcholinesterase: catalytic processes mediated by aromatic and polar residues of the active centre

Neoceptor Concept Based on Molecular Complementarity in GPCRs: A Mutant Adenosine A3 Receptor with Selectively Enhanced Affinity for Amine-Modified Nucleosides

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