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...

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Bibliografski detalji
Glavni autori: Smallridge, R, Whiteman, P, Werner, J, Campbell, I, Handford, P, Downing, A
Format: Journal article
Jezik:English
Izdano: 2003

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