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Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

From: Identification and in silico analysis of a spectrum of SLC4A11 variations in Indian familial and sporadic cases of congenital hereditary endothelial dystrophy

Fig. 3

3A, 3B, 3C shows modelled WT SLC4A11 structures in which zone around site of alteration is analysed. 3A1, 3B1,3C1 shows focused zone around WD residue and 3A2,3B2,3C2 shows corresponding focused zone around altered residue for S489W, R869C and S480I variations respectively (encircled). Number of amino acid residue clashes in surrounding zone was found two in S489W, zero in R869C and two in S480I

Homology-based protein modelling of SLC4A11 protein and structural analysis.

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