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. 1998 Oct;180(19):5077–5084. doi: 10.1128/jb.180.19.5077-5084.1998

FIG. 1.

FIG. 1

Locations of restriction sites in B. megaterium gpr and possible catalytic residues in B. megaterium GPR (A) and amino acid sequences of B. megaterium GPR variants (B). (A) The locations of restriction sites and codons for possible catalytic residues in B. megaterium gpr were taken from reference 30. The locations of codons for possible catalytic residues are given above the gene (open box), and restriction sites (C1, ClaI; E1, EagI; H2, HincII; H3, HindIII; NcI, NcoI; NrI, NruI) are indicated below the gene. N and C denote the N- and C-terminal coding regions, respectively. Note that the HincII and HindIII sites are outside the gpr gene’s coding sequence. The arrow labeled ΔP39 denotes the region in which P41 autoprocesses to P39. (B) Amino acid sequences (in one-letter code) of various forms of GPR. The sequences of P46 and P41 (note that this is P41 overexpressed in E. coli) are from references 6 and 24. The sequence of ΔP39 is from this work, and those of the variants lacking 3 to 12 propeptide residues are from reference 17. The numbers above the sequences are the positions of lysine or arginine residues in P46; arrows labeled P41 and P39 denote the sites of cleavage generating P41 and P39, respectively.