Molecular modelling of the C-terminal domains of factor H of human complement: A correlation between haemolytic uraemic syndrome and a predicted heparin binding site

Journal of Molecular Biology

Volumn 316, Issue 2, 2002, Pages 217-224

  Perkins, Stephen J ^a   Goodship, Timothy H J ^b  

^a ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

Factor H; Fibroblast growth factor; Haemolytic uraemic syndrome; Heparin; Molecular graphics

Indexed keywords

ACIDIC FIBROBLAST GROWTH FACTOR; COMPLEMENT COMPONENT C3B; COMPLEMENT FACTOR H; FIBRINOGEN; HEPARIN; POLYANION;

AMINO ACID COMPOSITION; AMINO ACID SUBSTITUTION; ARTICLE; BINDING SITE; CARBOXY TERMINAL SEQUENCE; CELL SURFACE; COMPLEMENT BLOOD LEVEL; COMPLEMENT SYSTEM; COMPLEX FORMATION; CONTROLLED STUDY; CORRELATION ANALYSIS; CRYSTAL STRUCTURE; HEMOLYTIC UREMIC SYNDROME; HUMAN; KIDNEY; MISSENSE MUTATION; MOLECULAR MODEL; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; PROTEIN BINDING; PROTEIN DEFECT; PROTEIN DEGRADATION; PROTEIN DOMAIN; PROTEIN FUNCTION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; PROTEIN STRUCTURE; REGULATORY MECHANISM;

EID: 0036289142     PISSN: 00222836     EISSN: None     Source Type: Journal    
DOI: 10.1006/jmbi.2001.5337     Document Type: Article

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