How do rotameric conformations influence the time-resolved fluorescence of tryptophan in proteins? A perspective based on molecular modeling and Quantum Chemistry

Current Protein and Peptide Science

Volumn 9, Issue 5, 2008, Pages 427-446

  Moors, Samuel L C ^a   Jonckheer, Abel ^a   De Maeyer, Marc ^a   Engelborghs, Yves ^a   Ceulemans, Arnout ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

Dead end elimination; Molecular dynamics; Rotamer model; Tryptophan excited state; Tryptophan photophysics

Indexed keywords

5 FLUOROTRYPTOPHAN; ACRYLAMIDE; AMINO ACID; PARVALBUMIN; TRYPTOPHAN; UNCLASSIFIED DRUG; PROTEIN;

ACCURACY; ANISOTROPY; CHROMATOPHORE; CONCEPTUAL FRAMEWORK; ELECTRON TRANSPORT; FIELD EMISSION; FLAME PHOTOMETRY; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; LIGAND BINDING; MACROMOLECULE; MATHEMATICAL ANALYSIS; MOLECULAR DYNAMICS; MOLECULAR EVOLUTION; MOLECULAR MECHANICS; MOLECULAR MODEL; NUCLEAR MAGNETIC RESONANCE; PHOTOCHEMICAL QUENCHING; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN POLYMORPHISM; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; PROTON TRANSPORT; QUANTUM CHEMISTRY; QUANTUM MECHANICS; REVIEW; SOLVATION; THERMODYNAMICS; X RAY CRYSTALLOGRAPHY; CHEMICAL MODEL; CHEMICAL STRUCTURE; CHEMISTRY; COMPUTER SIMULATION; CONFORMATION; ELECTRICITY; KINETICS; PROTEIN SECONDARY STRUCTURE; QUANTUM THEORY; SOLUTION AND SOLUBILITY;

ANISOTROPY; COMPUTER SIMULATION; ELECTROSTATICS; FLUORESCENCE; KINETICS; MODELS, CHEMICAL; MODELS, MOLECULAR; MOLECULAR CONFORMATION; PROTEIN STRUCTURE, SECONDARY; PROTEINS; QUANTUM THEORY; SOLUTIONS; THERMODYNAMICS; TRYPTOPHAN;

EID: 55949111379     PISSN: 13892037     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920308785915236     Document Type: Review

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