Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA - Wikidata - awgldk - TriplyDB

Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA

Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA

http://www.wikidata.org/entity/Q27622627

about

Interaction of the herbicide glyphosate with its target enzyme 5-enolpyruvylshikimate 3-phosphate synthase in atomic detail Closing down on glyphosate inhibition--with a new structure for drug discovery Crystal structure of human L-isoaspartyl-O-methyl-transferase with S-adenosyl homocysteine at 1.6-A resolution and modeling of an isoaspartyl-containing peptide at the active site Structure-function relationships in methionine adenosyltransferases Fluorescence of covalently attached pyrene as a general RNA folding probe.Resistance to antibiotics targeted to the bacterial cell wall A new view of the mechanisms of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) and 5-enolpyruvylshikimate-3-phosphate synthase (AroA) derived from X-ray structures of their tetrahedral reaction intermediate states Discovery of a Potential Allosteric Ligand Binding Site in CDK2 Structural and Functional Characterization of NikO, an Enolpyruvyl Transferase Essential in Nikkomycin Biosynthesis Characterization of a Phanerochaete chrysosporium Glutathione Transferase Reveals a Novel Structural and Functional Class with Ligandin Properties Functional Consequence of Covalent Reaction of Phosphoenolpyruvate with UDP-N-acetylglucosamine 1-Carboxyvinyltransferase (MurA)Diversification of fungal specific class a glutathione transferases in saprotrophic fungi Latest methods of fluorescence-based protein crystal identification Binding of polarity-sensitive hydrophobic ligands to erythroid and nonerythroid spectrin: fluorescence and molecular modeling studies.A thermodynamic characterization of the interaction of 8-anilino-1-naphthalenesulfonic acid with native globular proteins: the effect of the ligand dimerization in the analysis of the binding isotherms.Structural and functional evolution of positively selected sites in pine glutathione S-transferase enzyme family Functional divergence and catalytic properties of dehydroascorbate reductase family proteins from Populus tomentosa.Folding of dimeric methionine adenosyltransferase III: identification of two folding intermediates.Inhibition of protein aggregation: supramolecular assemblies of arginine hold the key Reevaluation of ANS binding to human and bovine serum albumins: key role of equilibrium microdialysis in ligand - receptor binding characterization 1-Anilino-8-naphthalene sulfonate (ANS) is not a desirable probe for determining the molten globule state of chymopapain The bacterial cell wall as a source of antibacterial targets.Direct determination of multiple ligand interactions with the extracellular domain of the calcium-sensing receptor.Phosphorylation in the catalytic cleft stabilizes and attracts domains of a phosphohexomutase Atomic force microscopy study of the conformational change in immobilized calmodulin.Characterization of the binding of 8-anilinonaphthalene sulfonate to rat class Mu GST M1-1.Cytoplasmic steps of peptidoglycan biosynthesis.Regulated structural transitions unleash the chaperone activity of αB-crystallin Metal deficiency increases aberrant hydrophobicity of mutant superoxide dismutases that cause amyotrophic lateral sclerosis S-nitrosylation of UCHL1 induces its structural instability and promotes α-synuclein aggregation.Peptidoglycan biosynthesis machinery: a rich source of drug targets.Evidence that the fosfomycin target Cys115 in UDP-N-acetylglucosamine enolpyruvyl transferase (MurA) is essential for product release.UDP-N-acetylglucosamine enolpyruvyl transferase as a potential target for antibacterial chemotherapy: recent developments.Biophysical and folding parameters of trypanothione reductase from Leishmania infantum.Exploring the Transition of Human α-Synuclein from Native to the Fibrillar State: Insights into the Pathogenesis of Parkinson's Disease.Characterization of fluorescence of ANS-tear lipocalin complex: evidence for multiple-binding modes.The Effect of Surface Charge Saturation on Heat-induced Aggregation of Firefly Luciferase.ANS fluorescence: potential to augment the identification of the external binding sites of proteins.A novel inhibitor that suspends the induced fit mechanism of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA).A conserved N-capping motif contributes significantly to the stabilization and dynamics of the C-terminal region of class Alpha glutathione S-transferases.

P2860

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P2860

Structural basis for the interaction of the fluorescence probe 8-anilino-1-naphthalene sulfonate (ANS) with the antibiotic target MurA

http://www.wikidata.org/entity/Q27622627

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2000 nî lūn-bûn

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2000 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2000年の論文

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P2860

Improved methods for building protein models in electron density maps and the location of errors in these models

Crystallography & NMR System: A New Software Suite for Macromolecular Structure Determination

PROCHECK: a program to check the stereochemical quality of protein structures

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

Processing of X-ray diffraction data collected in oscillation mode

Role of the loop containing residue 115 in the induced-fit mechanism of the bacterial cell wall biosynthetic enzyme MurA

Structure and topological symmetry of the glyphosate target 5-enolpyruvylshikimate-3-phosphate synthase: a distinctive protein fold

Functional mimicry of a protein hormone by a peptide agonist: the EPO receptor complex at 2.8 A

Crystal structure of UDP-N-acetylglucosamine enolpyruvyltransferase, the target of the antibiotic fosfomycin

Structure of UDP-N-acetylglucosamine enolpyruvyl transferase, an enzyme essential for the synthesis of bacterial peptidoglycan, complexed with substrate UDP-N-acetylglucosamine and the drug fosfomycin

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