Prokaryotic ubiquitin-like protein


Prokaryotic ubiquitin-like protein is a functional analog of ubiquitin found in the prokaryote Mycobacterium tuberculosis. Modification with Pup is called pupylation. Pup serves the same function as ubiquitin, although the enzymology of ubiquitylation and pupylation is different. In contrast to the three-step reaction of ubiquitylation, pupylation requires two steps, therefore only two enzymes are involved in pupylation. Similar to ubiquitin, Pup attaches to specific lysine residues of substrate proteins by forming isopeptide bonds. It is then recognized by Mycobacterium proteasomal ATPase by a binding-induced folding mechanism that forms a unique alpha-helix. Mpa then delivers the Pup-substrate to the 20S proteasome by coupling of ATP hydrolysis for proteasomal degradation.
The discovery of Pup indicates that like eukaryotes, bacteria may use a small-protein modifier to control protein stability.
The X-ray crystal structure of the Pup/Mpa complex has been determined.
The Pup gene encodes a 64–amino acid protein with a molecular size of 6.944 kDa:
In 2017, the presence of Pup homologs in bacterial species outside of the group of gram-positive bacteria was reported. The Pup homologs were termed UBact, although the distinction has not been proven to be phylogenetically supported by a separate evolutionary origin and is without experimental evidence. UBact is a homolog of Pup, and is found in several phyla of gram-negative bacteria. Below is the UBact sequence in the bacterium Methylacidiphilum infernorum: