About the structural role of disulfide bridges in serum albumins: Evidence from protein simulated unfolding

Biopolymers

Volumn 97, Issue 11, 2012, Pages 889-898

  Paris, Guillaume ^a   Kraszewski, Sebastian ^b   Ramseyer, Christophe ^b   Enescu, Mironel ^a  

^a UNIVERSITÉ DE FRANCHE COMTÉ   (France)

^b UNIVERSITY HOSPITAL OF BESANÇON   (France)

Author keywords

AMBER ff03; helicity; MD simulation; native contacts; OPLS AA; S S bridge

Indexed keywords

CLASSICAL MOLECULAR DYNAMICS; CONFORMATIONAL TRANSITIONS; CYSTEINE RESIDUES; DISULFIDE BRIDGE; EXPERIMENTAL DATA; FORCE FIELDS; GYRATION RADII; HELICITIES; HUMAN SERUM ALBUMINS; MD SIMULATION; NATIVE CONFORMATION; OPLS-AA; PEPTIDE CHAIN; POTENTIAL WELLS; PROTEIN SECONDARY STRUCTURE; PROTEIN STRUCTURES; SERUM ALBUMIN; SIMULATION METHODS; TERTIARY STRUCTURES; THEORETICAL RESULT; THERMAL UNFOLDING;

AMBER; AMINO ACIDS; COVALENT BONDS; MOLECULAR DYNAMICS; STRUCTURE (COMPOSITION);

PROTEINS;

DISULFIDE; HUMAN SERUM ALBUMIN;

ALPHA HELIX; ARTICLE; MOLECULAR DYNAMICS; PROTEIN CONFORMATION; PROTEIN FOLDING; PROTEIN SECONDARY STRUCTURE; PROTEIN STRUCTURE; PROTEIN TERTIARY STRUCTURE;

CYSTEINE; DISULFIDES; HUMANS; KINETICS; MOLECULAR DYNAMICS SIMULATION; OXIDATION-REDUCTION; PROTEIN FOLDING; PROTEIN STABILITY; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; SERUM ALBUMIN; TEMPERATURE; THERMODYNAMICS;

EID: 84865115865     PISSN: 00063525     EISSN: 10970282     Source Type: Journal    
DOI: 10.1002/bip.22096     Document Type: Article

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