A bstract The prediction of protein structure and the design of novel protein sequences and structures have long been intertwined. The recently released AlphaFold has heralded a new generation of accurate protein structure prediction, but the extent to which this affects protein design stands yet unexplored. Here we develop a rapid and effective approach for fixed backbone computational protein design, leveraging the predictive power of AlphaFold. For several designs we demonstrate that not only are the AlphaFold predicted structures in agreement with the desired backbones, but they are also supported by the structure predictions of other supervised methods as well as ab initio folding. These results suggest that AlphaFold, and methods like it, are able to facilitate the development of a new range of novel and accurate protein design methodologies.