(a) The proximal centriole was characterized by complete triplet microtubules that showed strong density for both parts of the A-C linker (white double arrowheads) and the pinhead (green arrow). (b) In contrast, the distal centriole lacked the A-C linker (white double arrowheads) and instead of a pinhead, the distal map had a density (green arrow) that extended out from the A-tubule. (c) A merge of the distal and proximal maps highlighted the differences between them, with differences at the inner AB-junction (white arrow) being the most obvious. (d) A zoomed in view of the A-tubule in the proximal centriole showed two MIPs, one straddling protofilaments A09 and A10, the other binding to A11. Note that the inner AB-junction is compact (dashed white circle). (e) A zoomed in view of the A-tubule in the distal centriole also showed a MIP straddling protofilaments A09-A10, but the proximal centriole lacked the A11-bound MIP. Here the inner AB-junction was more elaborate and formed the platform from which densities extended (dashed white circle). (f) A merged view of both A-tubules allows the differences at the inner AB-junction to be fully appreciated. Scale bars are 25 nm.