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. Author manuscript; available in PMC: 2011 Jun 29.
Published in final edited form as: Biochemistry. 2010 Jun 29;49(25):5083–5085. doi: 10.1021/bi100235z

Figure 1.

Figure 1

Ribbon diagram of the p150Glued CAP-gly domain (yellow) bound to EB1 (cyan). The point mutations identified in Perry’s syndrome are shown as sticks in magenta. These mutations are located in a long loop that connects β3 and β4 strands and part of the ‘GKNDG’ binding motif. The location of G59 is also shown.