| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| defB | rseP | BSU14560 | BSU16560 | Formylmethionine deformylase A; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | Regulator of sigma-W protease RasP; Is responsible for site-2 cleavage of the RsiW anti-sigma factor. This results, after a third proteolytic step catalyzed by the ClpXP protease, in the release of SigW and the transcription activation of the genes under the control of the sigma-W factor. Can also cleave liberated signal peptides of PenP and Mpr, probably within in the cell membrane. | 0.442 |
| defB | ydiL | BSU14560 | BSU06010 | Formylmethionine deformylase A; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | Putative membrane protease; May function as endopeptidase which proteolytically removes the C-terminal three residues of farnesylated peptides containing the CAAX motif where C is cysteine, A is an aliphatic amino acid and X is any amino acid; Belongs to the peptidase U48 family. | 0.505 |
| defB | yoyI | BSU14560 | BSU20929 | Formylmethionine deformylase A; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function. | 0.519 |
| pbpF | rseP | BSU10110 | BSU16560 | Penicillin-binding protein 2C required for spore germination; Cell wall formation. May be involved in outgrowth of the germinated spore or it could function in the synthesis of the germ cell wall; In the N-terminal section; belongs to the glycosyltransferase 51 family. | Regulator of sigma-W protease RasP; Is responsible for site-2 cleavage of the RsiW anti-sigma factor. This results, after a third proteolytic step catalyzed by the ClpXP protease, in the release of SigW and the transcription activation of the genes under the control of the sigma-W factor. Can also cleave liberated signal peptides of PenP and Mpr, probably within in the cell membrane. | 0.748 |
| pbpF | yoyI | BSU10110 | BSU20929 | Penicillin-binding protein 2C required for spore germination; Cell wall formation. May be involved in outgrowth of the germinated spore or it could function in the synthesis of the germ cell wall; In the N-terminal section; belongs to the glycosyltransferase 51 family. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function. | 0.451 |
| rseP | defB | BSU16560 | BSU14560 | Regulator of sigma-W protease RasP; Is responsible for site-2 cleavage of the RsiW anti-sigma factor. This results, after a third proteolytic step catalyzed by the ClpXP protease, in the release of SigW and the transcription activation of the genes under the control of the sigma-W factor. Can also cleave liberated signal peptides of PenP and Mpr, probably within in the cell membrane. | Formylmethionine deformylase A; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | 0.442 |
| rseP | pbpF | BSU16560 | BSU10110 | Regulator of sigma-W protease RasP; Is responsible for site-2 cleavage of the RsiW anti-sigma factor. This results, after a third proteolytic step catalyzed by the ClpXP protease, in the release of SigW and the transcription activation of the genes under the control of the sigma-W factor. Can also cleave liberated signal peptides of PenP and Mpr, probably within in the cell membrane. | Penicillin-binding protein 2C required for spore germination; Cell wall formation. May be involved in outgrowth of the germinated spore or it could function in the synthesis of the germ cell wall; In the N-terminal section; belongs to the glycosyltransferase 51 family. | 0.748 |
| rseP | yoyI | BSU16560 | BSU20929 | Regulator of sigma-W protease RasP; Is responsible for site-2 cleavage of the RsiW anti-sigma factor. This results, after a third proteolytic step catalyzed by the ClpXP protease, in the release of SigW and the transcription activation of the genes under the control of the sigma-W factor. Can also cleave liberated signal peptides of PenP and Mpr, probably within in the cell membrane. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function. | 0.450 |
| xkdB | xkdC | BSU12520 | BSU12530 | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | 0.998 |
| xkdB | ycgE | BSU12520 | BSU03080 | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | Putative transcriptional regulator; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type pr: putative regulator. | 0.488 |
| xkdB | ydiL | BSU12520 | BSU06010 | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | Putative membrane protease; May function as endopeptidase which proteolytically removes the C-terminal three residues of farnesylated peptides containing the CAAX motif where C is cysteine, A is an aliphatic amino acid and X is any amino acid; Belongs to the peptidase U48 family. | 0.455 |
| xkdB | yonH | BSU12520 | BSU21090 | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | Putative capsid protein; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type ps: putative structure. | 0.403 |
| xkdB | yoyI | BSU12520 | BSU20929 | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function. | 0.621 |
| xkdC | xkdB | BSU12530 | BSU12520 | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | 0.998 |
| xkdC | ycgE | BSU12530 | BSU03080 | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | Putative transcriptional regulator; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type pr: putative regulator. | 0.488 |
| xkdC | ydiL | BSU12530 | BSU06010 | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | Putative membrane protease; May function as endopeptidase which proteolytically removes the C-terminal three residues of farnesylated peptides containing the CAAX motif where C is cysteine, A is an aliphatic amino acid and X is any amino acid; Belongs to the peptidase U48 family. | 0.458 |
| xkdC | yonH | BSU12530 | BSU21090 | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | Putative capsid protein; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type ps: putative structure. | 0.505 |
| xkdC | yoyI | BSU12530 | BSU20929 | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function. | 0.621 |
| ycgE | xkdB | BSU03080 | BSU12520 | Putative transcriptional regulator; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type pr: putative regulator. | Conserved hypothetical protein; Evidence 4: Homologs of previously reported genes of unknown function; To B.subtilis YqaL. | 0.488 |
| ycgE | xkdC | BSU03080 | BSU12530 | Putative transcriptional regulator; Evidence 3: Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; Product type pr: putative regulator. | Conserved hypothetical protein in PBSX phage element; May function as a transcriptional antiterminator. | 0.488 |