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. 2017 Aug 18;11(6):499–501. doi: 10.1080/19336950.2017.1357944

Figure 1.

Figure 1.

The ROMK immunoglobulin-like domain with select residues mutated in Bartter syndrome are highlighted. Mutations tested in the recently published study: A198T (yellow), R212P (purple), H270Y (orange), Y314C (red). Other mutations of interest and discussed in the text: I211S (green), S276N (cyan), L297S (dark blue). Representations rendered with PyMol molecular graphics system version 1.8.