Once you have the different sequences (from the blast, as suggested by Michael J. Benedik: https://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE=Proteins), you can aligne them with Clustal omega (https://www.ebi.ac.uk/Tools/msa/clustalo/) to see if some portions of you sequences are missing.
As Michael and Katy suggested, a simple blast search of the annotated genome sequences with your sequence of interest should identify the other related sequences, either full-length or truncated.
If you want to know the copy number of gene in bacteria you shuold use gene expression by using qPCR thats depend on you if like to use syber green or taq man method. If you have sequence for the target gene you can use NCBI Aliment by using blast
Just a small addition on the other people useful answers. When you perform your blast I would use tblastn to blast the protein you are interested in against the bacterial genome. Due to evolution you gene sequence may have been diverged and looking for the protein would give you more reliable results. Once you find the region where your protein return a hit you should also check for any stop codon interrupting the coding sequence or eventually some small intel that can cause a frameshift.