Structure-function-folding relationships and native energy landscape of dynein light chain protein: Nuclear magnetic resonance insights

Journal of Biosciences

Volumn 34, Issue 3, 2009, Pages 465-479

  Krishna Mohan, P M ^a,b   Hosur, Ramakrishna V ^a  

^a TATA INSTITUTE OF FUNDAMENTAL RESEARCH   (India)

^b RUTGERS UNIVERSITY   (United States)

Author keywords

Cargo trafficking; Dynein light chain protein; Monomeric intermediate; Native energy landscape; Nuclear magnetic resonance

Indexed keywords

CYTOPLASMIC DYNEIN; OLIGOPEPTIDE;

AMINO ACID SEQUENCE; CHEMICAL STRUCTURE; CHEMISTRY; DIMERIZATION; HEAT; HYDROGEN BOND; HYDROPHOBICITY; METABOLISM; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE; PH; PHYSICAL PHENOMENA; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN DENATURATION; PROTEIN FOLDING; PROTEIN SECONDARY STRUCTURE; PROTEIN TERTIARY STRUCTURE; REVIEW; STRUCTURE ACTIVITY RELATION; THERMODYNAMICS;

AMINO ACID SEQUENCE; CYTOPLASMIC DYNEINS; DIMERIZATION; HOT TEMPERATURE; HYDROGEN BONDING; HYDROGEN-ION CONCENTRATION; HYDROPHOBICITY; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; OLIGOPEPTIDES; PHYSICAL PROCESSES; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN DENATURATION; PROTEIN FOLDING; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; STRUCTURE-ACTIVITY RELATIONSHIP; THERMODYNAMICS;

EID: 73449105815     PISSN: 02505991     EISSN: 09737138     Source Type: Journal    
DOI: 10.1007/s12038-009-0052-0     Document Type: Review

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