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. Author manuscript; available in PMC: 2018 Sep 25.
Published in final edited form as: Expert Opin Orphan Drugs. 2017 Sep 25;5(10):813–825. doi: 10.1080/21678707.2017.1375403

Figure 2.

Figure 2

CXCR4 evolution and mutations. The amino acid sequence of the C-tail region of wild type CXCR4 is aligned with the corresponding sequence from variants found in patients with WHIM syndrome. The circle locates the single amino acid substitution found in mutation E343K. The underlined sequence denotes de novo sequence imposed by frame shifts.