FIGURE 3:

Preventing averaging of α- and β-tubulin by kinesin decoration does not reveal any difference between acetylation states. (A) End-on view of the deacetylated, dynamic microtubule reconstruction with kinesin. (B) Inside and (C) outside views of an isolated tubulin dimer, with differences superimposed as in Figure 2. No significant differences were observed within the tubulin dimer. The location of the loop containing the modified residue is indicated by the circle. α-Tubulin is shown in green, β-tubulin in blue, and kinesin (1BG2) in purple.