Search Results - "Barak, Dov"
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Identification by Site-directed Mutagenesis of Residues Involved in Ligand Recognition and Activation of the Human A3 Adenosine Receptor
Published in The Journal of biological chemistry (24-05-2002)“…Ligand recognition has been extensively explored in G protein-coupled A1, A2A, and A2B adenosine receptors but not in the A3receptor, which is…”
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Crystal Structures of Aged Phosphonylated Acetylcholinesterase: Nerve Agent Reaction Products at the Atomic Level
Published in Biochemistry (Easton) (01-06-1999)“…Organophosphorus acid anhydride (OP) nerve agents are potent inhibitors which rapidly phosphonylate acetylcholinesterase (AChE) and then may undergo an…”
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3
Functional Characteristics of the Oxyanion Hole in Human Acetylcholinesterase
Published in The Journal of biological chemistry (31-07-1998)“…The contribution of the oxyanion hole to the functional architecture and to the hydrolytic efficiency of human acetylcholinesterase (HuAChE) was investigated…”
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4
Constitutive Activation of A3 Adenosine Receptors by Site-Directed Mutagenesis
Published in Biochemical and biophysical research communications (15-06-2001)“…The objective of this study was to create constitutively active mutant human A3 adenosine receptors (ARs) using single amino acid replacements, based on…”
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The Architecture of Human Acetylcholinesterase Active Center Probed by Interactions with Selected Organophosphate Inhibitors
Published in The Journal of biological chemistry (17-05-1996)“…The role of the functional architecture of human acetylcholinesterase (HuAChE) active center in facilitating reactions with organophosphorus inhibitors was…”
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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 (∗)
Published in The Journal of biological chemistry (03-02-1995)“…Substitution of Trp-86, in the active center of human acetylcholinesterase (HuAChE), by aliphatic but not by aromatic residues resulted in a several…”
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Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A2A Adenosine Receptor Crystallographic Structure
Published in Journal of medicinal chemistry (28-05-2009)“…Homology modeling of the human A2A adenosine receptor (AR) based on bovine rhodopsin predicted a protein structure that was very similar to the recently…”
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Evaluation of homology modeling of G-protein-coupled receptors in light of the A(2A) adenosine receptor crystallographic structure
Published in Journal of medicinal chemistry (28-05-2009)“…Homology modeling of the human A(2A) adenosine receptor (AR) based on bovine rhodopsin predicted a protein structure that was very similar to the recently…”
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Carbocation-Mediated Processes in Biocatalysts. Contribution of Aromatic Moieties
Published in Journal of the American Chemical Society (02-04-1997)Get full text
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A preliminary comparison of structural models for catalytic intermediates of acetylcholinesterase
Published in Chemico-biological interactions (14-05-1999)“…Determination of the three dimensional structure of Torpedo Californica acetylcholinesterase (TcAChE) provided an experimental tool for directly visualizing…”
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Ligand-G Protein Allosteric Communication through Internal Waters in GPCR Complexes
Published in Biophysical journal (27-01-2015)Get full text
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12
The Role of Internal Water in GPCR Complexes
Published in Biophysical journal (29-01-2013)Get full text
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Direct determination of the chemical composition of acetylcholinesterase phosphonylation products utilizing electrospray-ionization mass spectrometry
Published in FEBS letters (05-05-1997)“…While non-reactivability of cholinesterases from their phosphyl conjugates (aging) is attributed to an unimolecular process involving loss of alkyl group from…”
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Accommodation of physostigmine and its analogues by acetylcholinesterase is dominated by hydrophobic interactions
Published in Biochemical journal (01-01-2009)“…The role of the functional architecture of the HuAChE (human acetylcholinesterase) in reactivity toward the carbamates pyridostigmine, rivastigmine and several…”
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Evaluation of Homology Modeling of G-Protein-Coupled Receptors in Light of the A 2A Adenosine Receptor Crystallographic Structure
Published in Journal of medicinal chemistry (28-05-2009)Get full text
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16
Structural Determinants of A3 Adenosine Receptor Activation: Nucleoside Ligands at the Agonist/Antagonist Boundary
Published in Journal of medicinal chemistry (26-09-2002)“…Mutagenesis of the human A3 adenosine receptor (AR) suggested that certain amino acid residues contributed differently to ligand binding and activation…”
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Structural determinants of A(3) adenosine receptor activation: nucleoside ligands at the agonist/antagonist boundary
Published in Journal of medicinal chemistry (26-09-2002)“…Mutagenesis of the human A(3) adenosine receptor (AR) suggested that certain amino acid residues contributed differently to ligand binding and activation…”
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Function-specific blockage of M1 and M3 muscarinic acetylcholine receptors by VX and echothiophate
Published in Brain research (26-04-2006)Get full text
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Flexibility versus “rigidity” of the functional architecture of AChE active center
Published in Chemico-biological interactions (25-09-2008)“…Functional architecture of the AChE active center appears to be characterized by both structural “rigidity”, necessary to stabilize the catalytic triad as well…”
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Efficacy and Safety of Intravenous Immunoglobulin in Patients with Metastatic Melanoma
Published in Annals of the New York Academy of Sciences (01-09-2007)“…: We have previously reported studies performed both in vitro and in laboratory animals, as well as a case study in humans, suggesting that intravenous…”
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