| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| SSA_0872 | SSA_0874 | SSA_0872 | SSA_0874 | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | 0.499 |
| SSA_0872 | dinG | SSA_0872 | SSA_0873 | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | ATP-dependent DNA helicase; 3'-5' exonuclease. | 0.727 |
| SSA_0872 | rodA | SSA_0872 | SSA_0875 | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | Rod shape determining protein (cell-cycle protein), putative; GC: 44.77%; Transporter classification TC:9.B.3.1.3. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.775. Curator(s): L. Ozaki, J. Alves; Protein involved in cell division; Belongs to the SEDS family. | 0.575 |
| SSA_0872 | thiJ | SSA_0872 | SSA_0876 | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | 4-methyl-5(B-hydroxyethyl)-thiazole monophosphate biosynthesis protein, putative; GC: 47.18%; Codon Adaptation Index (CAI): 0.804. Curator(s): L. Ozaki. | 0.462 |
| SSA_0874 | SSA_0872 | SSA_0874 | SSA_0872 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | 0.499 |
| SSA_0874 | SSA_0877 | SSA_0874 | SSA_0877 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | 0.532 |
| SSA_0874 | dinG | SSA_0874 | SSA_0873 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | ATP-dependent DNA helicase; 3'-5' exonuclease. | 0.724 |
| SSA_0874 | gyrB | SSA_0874 | SSA_0878 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | DNA gyrase, putative; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. | 0.551 |
| SSA_0874 | rodA | SSA_0874 | SSA_0875 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | Rod shape determining protein (cell-cycle protein), putative; GC: 44.77%; Transporter classification TC:9.B.3.1.3. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.775. Curator(s): L. Ozaki, J. Alves; Protein involved in cell division; Belongs to the SEDS family. | 0.841 |
| SSA_0874 | thiJ | SSA_0874 | SSA_0876 | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | 4-methyl-5(B-hydroxyethyl)-thiazole monophosphate biosynthesis protein, putative; GC: 47.18%; Codon Adaptation Index (CAI): 0.804. Curator(s): L. Ozaki. | 0.732 |
| SSA_0877 | SSA_0874 | SSA_0877 | SSA_0874 | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | 0.532 |
| SSA_0877 | dinG | SSA_0877 | SSA_0873 | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | ATP-dependent DNA helicase; 3'-5' exonuclease. | 0.515 |
| SSA_0877 | gyrB | SSA_0877 | SSA_0878 | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | DNA gyrase, putative; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. | 0.841 |
| SSA_0877 | rodA | SSA_0877 | SSA_0875 | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | Rod shape determining protein (cell-cycle protein), putative; GC: 44.77%; Transporter classification TC:9.B.3.1.3. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.775. Curator(s): L. Ozaki, J. Alves; Protein involved in cell division; Belongs to the SEDS family. | 0.617 |
| SSA_0877 | thiJ | SSA_0877 | SSA_0876 | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | 4-methyl-5(B-hydroxyethyl)-thiazole monophosphate biosynthesis protein, putative; GC: 47.18%; Codon Adaptation Index (CAI): 0.804. Curator(s): L. Ozaki. | 0.626 |
| dinG | SSA_0872 | SSA_0873 | SSA_0872 | ATP-dependent DNA helicase; 3'-5' exonuclease. | Zn-dependent hydrolases, including glyoxylases, putative; GC: 45.85%; Codon Adaptation Index (CAI): 0.773. Curator(s): L. Ozaki. | 0.727 |
| dinG | SSA_0874 | SSA_0873 | SSA_0874 | ATP-dependent DNA helicase; 3'-5' exonuclease. | Conserved membrane protein; GC: 44.34%; Transporter classification TC:9.B.63.1.2. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.756. SignalP prediction: Yes (prob. 0.998); Curator(s): L. Ozaki, J. Alves; (possible metabolite efflux protein), putative. | 0.724 |
| dinG | SSA_0877 | SSA_0873 | SSA_0877 | ATP-dependent DNA helicase; 3'-5' exonuclease. | Phosphoglycolate phosphatase, putative; GC: 43.58%; Codon Adaptation Index (CAI): 0.768. Curator(s): L. Ozaki; Protein involved in hydrolase activity. | 0.515 |
| dinG | gyrB | SSA_0873 | SSA_0878 | ATP-dependent DNA helicase; 3'-5' exonuclease. | DNA gyrase, putative; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. | 0.575 |
| dinG | rodA | SSA_0873 | SSA_0875 | ATP-dependent DNA helicase; 3'-5' exonuclease. | Rod shape determining protein (cell-cycle protein), putative; GC: 44.77%; Transporter classification TC:9.B.3.1.3. Transmembrane domains: 10. Codon Adaptation Index (CAI): 0.775. Curator(s): L. Ozaki, J. Alves; Protein involved in cell division; Belongs to the SEDS family. | 0.722 |