Being able to remove a restriction site by digesting with an enzyme that cuts at one site to linearize a plasmid, Klenow treating the linear fragment, then religating the fragment, is a useful trick in the lab. It can help you produce a suitable, and simple, cloning site when none previously existed in your vector. It is very simple to recreate this in your vector sequence using the Cloning Clipboard.
A new circular sequence will be created from your digested fragment.
The origin of your plasmid will have changed to the digested site, so you may want to rotate the sequence to match the original sequence.