Solution structure and dynamics of a calcium binding epidermal growth factor-like domain pair from the neonatal region of human fibrillin-1.
Fibrillin-1 is a mosaic protein mainly composed of 43 calcium binding epidermal growth factor-like (cbEGF) domains arranged as multiple, tandem repeats. Mutations within the fibrillin-1 gene cause Marfan syndrome (MFS), a heritable disease of connective tissue. More than 60% of MFS-causing mutations...
Hlavní autoři: | Smallridge, R, Whiteman, P, Werner, J, Campbell, I, Handford, P, Downing, A |
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Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2003
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