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...
المؤلفون الرئيسيون: | Smallridge, R, Whiteman, P, Werner, J, Campbell, I, Handford, P, Downing, A |
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التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2003
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مواد مشابهة
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A G1127S change in calcium-binding epidermal growth factor-like domain 13 of human fibrillin-1 causes short range conformational effects.
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منشور في: (2000) -
Fibrillin: from domain structure to supramolecular assembly.
حسب: Handford, P, وآخرون
منشور في: (2000)