Sonja Lorenz, Aaron J Cantor, Michael Rape and John Kuriyan
Abstract
The posttranslational modification of target proteins with ubiquitin and ubiquitin-like proteins is accomplished by the sequential action of E1, E2, and E3 enzymes. Members of the E1 and E3 enzyme families can undergo particularly large conformational changes during their catalytic cycles, involving the remodeling of domain interfaces. This enables the efficient, directed and regulated handover of ubiquitin from one carrier to the next one. We review some of
these conformational transformations, as revealed by crystallographic studies.
Download Full Article HERE
