| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| SBG_1600 | SBG_3200 | SBG_1600 | SBG_3200 | Conserved hypothetical protein. | Phage-like lysozyme. | 0.623 |
| SBG_1600 | bioH | SBG_1600 | SBG_3114 | Conserved hypothetical protein. | Putative biotin biosynthesis protein; The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters. | 0.439 |
| SBG_1600 | cls | SBG_1600 | SBG_1601 | Conserved hypothetical protein. | Cardiolipin synthetase; Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol. | 0.688 |
| SBG_1600 | gltB | SBG_1600 | SBG_2960 | Conserved hypothetical protein. | Glutamate synthase [NADPH] large chain precursor. | 0.539 |
| SBG_1600 | mreD | SBG_1600 | SBG_2990 | Conserved hypothetical protein. | Rod shape-determining protein; Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins. Belongs to the MreD family. | 0.484 |
| SBG_1600 | recX | SBG_1600 | SBG_2448 | Conserved hypothetical protein. | Putative regulatory protein RecX; Modulates RecA activity; Belongs to the RecX family. | 0.463 |
| SBG_1600 | tatA | SBG_1600 | SBG_3506 | Conserved hypothetical protein. | Sec-independent protein translocase protein. | 0.426 |
| SBG_1600 | tatB | SBG_1600 | SBG_3507 | Conserved hypothetical protein. | Sec-independent protein translocase protein; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation. | 0.440 |
| SBG_1600 | tatE | SBG_1600 | SBG_0540 | Conserved hypothetical protein. | Sec-independent protein translocase protein TatE; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. TatE shares overlapping functions with TatA; Belongs to the TatA/E family. TatE subfamily. | 0.587 |
| SBG_1600 | tonB | SBG_1600 | SBG_1599 | Conserved hypothetical protein. | TonB protein; Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy-requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins. Belongs to the TonB family. | 0.573 |
| SBG_3200 | SBG_1600 | SBG_3200 | SBG_1600 | Phage-like lysozyme. | Conserved hypothetical protein. | 0.623 |
| bioH | SBG_1600 | SBG_3114 | SBG_1600 | Putative biotin biosynthesis protein; The physiological role of BioH is to remove the methyl group introduced by BioC when the pimeloyl moiety is complete. It allows to synthesize pimeloyl-ACP via the fatty acid synthetic pathway through the hydrolysis of the ester bonds of pimeloyl-ACP esters. | Conserved hypothetical protein. | 0.439 |
| cls | SBG_1600 | SBG_1601 | SBG_1600 | Cardiolipin synthetase; Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol. | Conserved hypothetical protein. | 0.688 |
| gltB | SBG_1600 | SBG_2960 | SBG_1600 | Glutamate synthase [NADPH] large chain precursor. | Conserved hypothetical protein. | 0.539 |
| mreD | SBG_1600 | SBG_2990 | SBG_1600 | Rod shape-determining protein; Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins. Belongs to the MreD family. | Conserved hypothetical protein. | 0.484 |
| recX | SBG_1600 | SBG_2448 | SBG_1600 | Putative regulatory protein RecX; Modulates RecA activity; Belongs to the RecX family. | Conserved hypothetical protein. | 0.463 |
| tatA | SBG_1600 | SBG_3506 | SBG_1600 | Sec-independent protein translocase protein. | Conserved hypothetical protein. | 0.426 |
| tatA | tatB | SBG_3506 | SBG_3507 | Sec-independent protein translocase protein. | Sec-independent protein translocase protein; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation. | 0.999 |
| tatB | SBG_1600 | SBG_3507 | SBG_1600 | Sec-independent protein translocase protein; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation. | Conserved hypothetical protein. | 0.440 |
| tatB | tatA | SBG_3507 | SBG_3506 | Sec-independent protein translocase protein; Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin- arginine motif in their signal peptide across membranes. Together with TatC, TatB is part of a receptor directly interacting with Tat signal peptides. TatB may form an oligomeric binding site that transiently accommodates folded Tat precursor proteins before their translocation. | Sec-independent protein translocase protein. | 0.999 |