| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| KIQ64827.1 | KIQ67088.1 | TR51_11880 | TR51_06860 | Photosystem reaction center subunit H; Derived by automated computational analysis using gene prediction method: Protein Homology. | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.558 |
| KIQ64827.1 | KIQ67369.1 | TR51_11880 | TR51_06855 | Photosystem reaction center subunit H; Derived by automated computational analysis using gene prediction method: Protein Homology. | MerR family transcriptional regulator; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.472 |
| KIQ64827.1 | dinB | TR51_11880 | TR51_06845 | Photosystem reaction center subunit H; Derived by automated computational analysis using gene prediction method: Protein Homology. | DNA polymerase IV; Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII. | 0.428 |
| KIQ64827.1 | gcvP | TR51_11880 | TR51_06830 | Photosystem reaction center subunit H; Derived by automated computational analysis using gene prediction method: Protein Homology. | Glycine dehydrogenase; The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein; Belongs to the GcvP family. | 0.511 |
| KIQ67088.1 | KIQ64827.1 | TR51_06860 | TR51_11880 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Photosystem reaction center subunit H; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.558 |
| KIQ67088.1 | KIQ67089.1 | TR51_06860 | TR51_06870 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.724 |
| KIQ67088.1 | KIQ67090.1 | TR51_06860 | TR51_06875 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Membrane protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.662 |
| KIQ67088.1 | KIQ67369.1 | TR51_06860 | TR51_06855 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | MerR family transcriptional regulator; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.827 |
| KIQ67088.1 | KIQ67370.1 | TR51_06860 | TR51_06865 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | MerR family transcriptional regulator; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.830 |
| KIQ67088.1 | arc | TR51_06860 | TR51_15170 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | ATPase AAA; ATPase which is responsible for recognizing, binding, unfolding and translocation of pupylated proteins into the bacterial 20S proteasome core particle. May be essential for opening the gate of the 20S proteasome via an interaction with its C-terminus, thereby allowing substrate entry and access to the site of proteolysis. Thus, the C-termini of the proteasomal ATPase may function like a 'key in a lock' to induce gate opening and therefore regulate proteolysis. | 0.653 |
| KIQ67088.1 | dinB | TR51_06860 | TR51_06845 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | DNA polymerase IV; Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII. | 0.708 |
| KIQ67088.1 | eno | TR51_06860 | TR51_32680 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Enolase; Catalyzes the reversible conversion of 2-phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis; Belongs to the enolase family. | 0.541 |
| KIQ67088.1 | gcvP | TR51_06860 | TR51_06830 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Glycine dehydrogenase; The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein; Belongs to the GcvP family. | 0.565 |
| KIQ67088.1 | lon | TR51_06860 | TR51_34075 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Lon protease; ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short- lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner. | 0.541 |
| KIQ67089.1 | KIQ67088.1 | TR51_06870 | TR51_06860 | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.724 |
| KIQ67089.1 | KIQ67090.1 | TR51_06870 | TR51_06875 | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Membrane protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.511 |
| KIQ67089.1 | KIQ67369.1 | TR51_06870 | TR51_06855 | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | MerR family transcriptional regulator; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.774 |
| KIQ67089.1 | KIQ67370.1 | TR51_06870 | TR51_06865 | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | MerR family transcriptional regulator; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.835 |
| KIQ67089.1 | dinB | TR51_06870 | TR51_06845 | Signal peptide protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | DNA polymerase IV; Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII. | 0.511 |
| KIQ67090.1 | KIQ67088.1 | TR51_06875 | TR51_06860 | Membrane protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.662 |