Effects of tryptophan residue fluorination on streptavidin stability and biotin-streptavidin interactions via molecular dynamics simulations

Journal of Molecular Modeling

Volumn 15, Issue 3, 2009, Pages 257-266

  Panek, Jarosław J ^a,d   Ward, Thomas R ^b,c   Jezierska, Aneta ^d   Noviĉ, Marjana ^a  

^a NATIONAL INSTITUTE OF CHEMISTRY   (Slovenia)

^b UNIVERSITY OF NEUCHÂTEL   (Switzerland)

^c UNIVERSITY OF BASEL   (Switzerland)

^d UNIVERSITY OF WROC AW   (Poland)

Author keywords

Biotin; Fluorotryptophan; Molecular dynamics; Streptavidin; Thermodynamical perturbation

Indexed keywords

AVIDIN; BIOTIN; MUTANT PROTEIN; STREPTAVIDIN; TRYPTOPHAN;

ARTICLE; BINDING AFFINITY; COMPLEX FORMATION; FLUORINATION; HYDROGEN BOND; LIGAND BINDING; MATHEMATICAL COMPUTING; MOLECULAR DYNAMICS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN FOLDING; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; PROTEIN VARIANT; SIMULATION; SOLVENT EFFECT; THERMODYNAMICS; WILD TYPE;

BINDING SITES; BIOTIN; COMPUTER SIMULATION; CRYSTALLOGRAPHY, X-RAY; HALOGENATION; HYDROGEN BONDING; KINETICS; LIGANDS; MODELS, MOLECULAR; PROTEIN CONFORMATION; STREPTAVIDIN; THERMODYNAMICS; TRYPTOPHAN;

EID: 59149092144     PISSN: 16102940     EISSN: 09485023     Source Type: Journal    
DOI: 10.1007/s00894-008-0382-0     Document Type: Article

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