A hierarchy of functionally important relaxations within myoglobin based on solvent effects, mutations and kinetic model

Biochimica et Biophysica Acta - Proteins and Proteomics

Volumn 1749, Issue 2, 2005, Pages 234-251

  Dantsker, David ^a   Samuni, Uri ^a   Friedman, Joel M ^a   Agmon, Noam ^b  

^a ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

Conformational dynamics; Diffusion; Geminate recombination; Myoglobin; Relaxation; Sol gel; Trehalose

Indexed keywords

CARBON MONOXIDE; GLYCEROL; HEME; HISTIDINE; LEUCINE; LIGAND; MUTANT PROTEIN; MYOGLOBIN; SOLVENT; TREHALOSE; TRYPTOPHAN; XENON;

BINDING AFFINITY; BINDING SITE; CALCULATION; DATA ANALYSIS; ENERGY; GEL; KINETICS; LIGAND BINDING; METHODOLOGY; MODEL; MOTION; MUTATION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; REVIEW; TEMPERATURE; TEMPERATURE DEPENDENCE; THEORETICAL MODEL; TIME; WILD TYPE;

BINDING SITES; CARBON MONOXIDE; HEME; KINETICS; LIGANDS; MODELS, MOLECULAR; MODELS, THEORETICAL; MUTATION; MYOGLOBIN; PROTEIN BINDING; PROTEIN CONFORMATION; SOLVENTS; TREHALOSE;

ARRHENIUS;

EID: 20144364368     PISSN: 15709639     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbapap.2005.04.002     Document Type: Review

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