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Figure 8 | Orphanet Journal of Rare Diseases

Figure 8

From: Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy

Figure 8

Secondary structures prediction of ITGA7. (A) Secondary structures predictions for the ITGA7-882E (left) and ITGA7-882 K (right) proteins. The program also performed an accurate prediction of the real-valued relative solvent accessibility. The 882 E to K amino acid substitution changes the beta strands (green arrows) and alpha helix (red lines) structures of the ITGA7 protein. All changes are indicated with black arrows. (B) Enlarged area with the region containing the mutation highlighted.

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Orphanet Journal of Rare Diseases

ISSN: 1750-1172