| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| CH53_2205 | CH53_627 | CH53_2205 | CH53_627 | Hypothetical protein. | TPR repeat family protein. | 0.550 |
| CH53_2205 | maf-2 | CH53_2205 | CH53_2203 | Hypothetical protein. | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | 0.823 |
| CH53_2205 | mreB | CH53_2205 | CH53_2200 | Hypothetical protein. | Rod shape-determining protein mreB. | 0.479 |
| CH53_2205 | mreC | CH53_2205 | CH53_2201 | Hypothetical protein. | Rod shape-determining protein MreC; Involved in formation and maintenance of cell shape. | 0.608 |
| CH53_2205 | mreD | CH53_2205 | CH53_2202 | Hypothetical protein. | Rod shape-determining protein MreD; 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. | 0.878 |
| CH53_2205 | rng | CH53_2205 | CH53_2204 | Hypothetical protein. | Ribonuclease G. | 0.585 |
| CH53_627 | CH53_2205 | CH53_627 | CH53_2205 | TPR repeat family protein. | Hypothetical protein. | 0.550 |
| CH53_627 | mreD | CH53_627 | CH53_2202 | TPR repeat family protein. | Rod shape-determining protein MreD; 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. | 0.739 |
| CH53_627 | yfgA | CH53_627 | CH53_630 | TPR repeat family protein. | Helix-turn-helix family protein; Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis. | 0.657 |
| ftsL | mrdB | CH53_1025 | CH53_3063 | Cell division protein FtsL; Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. | Rod shape-determining protein RodA; Peptidoglycan polymerase that is essential for cell wall elongation; Belongs to the SEDS family. MrdB/RodA subfamily. | 0.868 |
| ftsL | mreC | CH53_1025 | CH53_2201 | Cell division protein FtsL; Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. | Rod shape-determining protein MreC; Involved in formation and maintenance of cell shape. | 0.418 |
| ftsL | mreD | CH53_1025 | CH53_2202 | Cell division protein FtsL; Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. | Rod shape-determining protein MreD; 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. | 0.706 |
| ftsL | yfgA | CH53_1025 | CH53_630 | Cell division protein FtsL; Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. | Helix-turn-helix family protein; Cytoskeletal protein that is involved in cell-shape control through regulation of the length of the long axis. | 0.629 |
| maf-2 | CH53_2205 | CH53_2203 | CH53_2205 | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | Hypothetical protein. | 0.823 |
| maf-2 | mreB | CH53_2203 | CH53_2200 | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | Rod shape-determining protein mreB. | 0.634 |
| maf-2 | mreC | CH53_2203 | CH53_2201 | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | Rod shape-determining protein MreC; Involved in formation and maintenance of cell shape. | 0.894 |
| maf-2 | mreD | CH53_2203 | CH53_2202 | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | Rod shape-determining protein MreD; 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. | 0.942 |
| maf-2 | rng | CH53_2203 | CH53_2204 | Septum formation protein Maf; Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | Ribonuclease G. | 0.890 |
| minC | mreB | CH53_3823 | CH53_2200 | Septum site-determining protein MinC; Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization; Belongs to the MinC family. | Rod shape-determining protein mreB. | 0.679 |
| minC | mreC | CH53_3823 | CH53_2201 | Septum site-determining protein MinC; Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization; Belongs to the MinC family. | Rod shape-determining protein MreC; Involved in formation and maintenance of cell shape. | 0.812 |