Small-angle X-ray scattering of apolipoprotein A-IV reveals the importance of its termini for structural stability

Journal of Biological Chemistry

Volumn 288, Issue 7, 2013, Pages 4854-4866

  Deng, Xiaodi ^a   Morris, Jamie ^b   Chaton, Catherine ^a   Schröder, Gunnar F ^c   Davidson, W Sean ^b   Thompson, Thomas B ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^b Metabolic Disease Institute   (United States)

^c FORSCHUNGSZENTRUM JÜLICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

APOLIPOPROTEINS; GLOBULAR DOMAINS; HELICAL BUNDLE; SMALL ANGLE X-RAY SCATTERING; STRUCTURAL INFORMATION; STRUCTURAL STABILITIES;

DIMERS; LIPOPROTEINS; STABILITY;

X RAY SCATTERING;

APOLIPOPROTEIN A4; DIMER; LIPID; MONOMER; PROLINE;

AMINO TERMINAL SEQUENCE; ARTICLE; BINDING AFFINITY; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; CRYSTAL STRUCTURE; DELETION MUTANT; HUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN ASSEMBLY; PROTEIN BINDING; PROTEIN CONFORMATION; PROTEIN LIPID INTERACTION; PROTEIN STABILITY; PROTEIN STRUCTURE; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

APOLIPOPROTEINS A; BIOPHYSICS; DIMERIZATION; DIMYRISTOYLPHOSPHATIDYLCHOLINE; HUMANS; LIPIDS; MOLECULAR CONFORMATION; POINT MUTATION; PROTEIN CONFORMATION; PROTEIN STRUCTURE, TERTIARY; SCATTERING, SMALL ANGLE; ULTRACENTRIFUGATION; X-RAYS;

EID: 84874050375     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.436709     Document Type: Article

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