Binding mechanism of an SH3 domain studied by NMR and ITC

Journal of the American Chemical Society

Volumn 131, Issue 12, 2009, Pages 4355-4367

  Demers, Jean Philippe ^a   Mittermaier, Anthony ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; AMINO ACIDS; DISSOCIATION; ENTHALPY; HYDROPHOBICITY; MAGNETIC DOMAINS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; RATE CONSTANTS;

ACTIVATION ENTHALPIES; ASSOCIATION RATE CONSTANTS; BINDING EQUILIBRIA; BINDING INTERFACE; BINDING MECHANISMS; BINDING REACTIONS; CONVENTIONAL METHODS; DIFFUSION LIMITED; DISSOCIATION ENTHALPIES; DISSOCIATION RATE CONSTANT; EYRING PLOT; HEAT CAPACITIES; HYDROPHOBIC CHARACTER; HYDROPHOBIC INTERFACE; INTERACTION MODEL; INTERMEDIATE STATE; ISOTHERMAL TITRATION CALORIMETRY; KINETIC CHARACTERIZATION; NMR DATA; NON-POLAR; SRC-HOMOLOGY; TEMPERATURE DEPENDENCE; TRANSITION STATE; TWO-STATE; TYROSINE KINASE;

NUCLEAR MAGNETIC RESONANCE;

FOCAL ADHESION KINASE 2; PROTEIN KINASE FYN; PROTEIN SH3; LIGAND; PEPTIDE;

ARTICLE; BINDING KINETICS; ENTROPY; HYDROPHOBICITY; ISOTHERMAL TITRATION CALORIMETRY; NUCLEAR MAGNETIC RESONANCE; PROTEIN ANALYSIS; PROTEIN DOMAIN; PROTEIN INTERACTION; TEMPERATURE; ANIMAL; BIOPHYSICS; CALORIMETRY; CHEMICAL PHENOMENA; CHEMISTRY; CHICKEN; KINETICS; MONTE CARLO METHOD; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PROCEDURES; PROTEIN TERTIARY STRUCTURE; STATISTICAL MODEL; THERMODYNAMICS;

ANIMALS; BIOPHYSICAL PROCESSES; CALORIMETRY; CHICKENS; HYDROPHOBIC AND HYDROPHILIC INTERACTIONS; KINETICS; LIGANDS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, STATISTICAL; MONTE CARLO METHOD; PEPTIDES; PROTEIN STRUCTURE, TERTIARY; PROTO-ONCOGENE PROTEINS C-FYN; TEMPERATURE; THERMODYNAMICS;

EID: 67849119942     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja808255d     Document Type: Article

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