Fibulin-3,-4, and-5 are highly susceptible to proteolysis, interact with cells and heparin, and form multimers

Journal of Biological Chemistry

Volumn 288, Issue 31, 2013, Pages 22821-22835

  Djokic, Jelena ^a   Fagotto Kaufmann, Christine ^b   Bartels, Rainer ^c   Nelea, Valentin ^a   Reinhardt, Dieter P ^a,b  

^a MCGILL UNIVERSITY   (Canada)

^b MCGILL UNIVERSITY   (Canada)

^c RESEARCH CENTER BORSTEL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ELASTOGENESIS; HEPARIN BINDING; MOLECULAR MECHANISM; MULTIMERIZATION; MULTIMERS; RGD MOTIF;

POLYSACCHARIDES;

ARGINYLGLYCYLASPARTIC ACID; CALCIUM; DIMER; DOXYCYCLINE; EPIDERMAL GROWTH FACTOR; FIBULIN; FIBULIN 3; FIBULIN 4; FIBULIN 5; GELATINASE A; GELATINASE B; HEPARAN SULFATE; HEPARIN; INTERSTITIAL COLLAGENASE; MACROPHAGE ELASTASE; MATRILYSIN; MONOMER; POLYMER; STROMELYSIN; UNCLASSIFIED DRUG;

AMINO TERMINAL SEQUENCE; ARTICLE; ATOMIC FORCE MICROSCOPY; BINDING SITE; CELL ADHESION; CELL INTERACTION; CELL SURFACE; CONTROLLED STUDY; DIMERIZATION; FIBROBLAST; GEL FILTRATION CHROMATOGRAPHY; HUMAN; HUMAN CELL; MASS SPECTROMETRY; NUCLEOTIDE SEQUENCE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN GLYCOSYLATION; PROTEIN MULTIMERIZATION; SMOOTH MUSCLE FIBER; WESTERN BLOTTING;

EID: 84881263823     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M112.439158     Document Type: Article

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