Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD)

Acta Crystallographica Section F: Structural Biology and Crystallization Communications

Volumn 65, Issue 7, 2009, Pages 665-670

  Magracheva, Eugenia ^a   Kozlov, Serguei ^b   Stewart, Colin L ^b,c   Wlodawer, Alexander ^b   Zdanov, Alexander ^a  

^a SAIC FREDERICK INC   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c INSTITUTE OF MEDICAL BIOLOGY   (Singapore)

Author keywords

Familial partial lipodystrophy; Lamin A C

Indexed keywords

DNA; LAMIN A; LAMIN C; MUTANT PROTEIN;

ALLOSTERISM; AMINO ACID SUBSTITUTION; ARTICLE; CHEMISTRY; DOMINANT GENE; FAMILIAL PARTIAL LIPODYSTROPHY; GENETICS; HUMAN; METABOLISM; MUTATION; PROTEIN BINDING; PROTEIN MULTIMERIZATION; PROTEIN QUATERNARY STRUCTURE; PROTEIN SECONDARY STRUCTURE; STATIC ELECTRICITY; X RAY CRYSTALLOGRAPHY;

ALLOSTERIC REGULATION; AMINO ACID SUBSTITUTION; CRYSTALLOGRAPHY, X-RAY; DNA; GENES, DOMINANT; HUMANS; LAMIN TYPE A; LIPODYSTROPHY, FAMILIAL PARTIAL; MUTANT PROTEINS; MUTATION; PROTEIN BINDING; PROTEIN MULTIMERIZATION; PROTEIN STRUCTURE, QUATERNARY; PROTEIN STRUCTURE, SECONDARY; STATIC ELECTRICITY;

EID: 68149083023     PISSN: 17443091     EISSN: 17443091     Source Type: Journal    
DOI: 10.1107/S1744309109020302     Document Type: Article

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