| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| dinB | ogt | CH53_2798 | CH53_4022 | 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. | methylated-DNA--protein-cysteine methyltransferase; Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction: the enzyme is irreversibly inactivated. | 0.423 |
| dinB | polA | CH53_2798 | CH53_1803 | 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. | Pola: DNA polymerase I. | 0.653 |
| dinB | rarA | CH53_2798 | CH53_165 | 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. | Replication-associated recombination protein A. | 0.483 |
| dinB | recQ | CH53_2798 | CH53_2009 | 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. | recQ: ATP-dependent DNA helicase RecQ. | 0.494 |
| ftsK | guaA | CH53_167 | CH53_620 | ftsK/SpoIIIE family protein. | GMP synthase; Catalyzes the synthesis of GMP from XMP. | 0.423 |
| ftsK | lolA | CH53_167 | CH53_166 | ftsK/SpoIIIE family protein. | Outer membrane lipocarrier protein LolA; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | 0.829 |
| ftsK | polA | CH53_167 | CH53_1803 | ftsK/SpoIIIE family protein. | Pola: DNA polymerase I. | 0.578 |
| ftsK | rarA | CH53_167 | CH53_165 | ftsK/SpoIIIE family protein. | Replication-associated recombination protein A. | 0.653 |
| ftsK | ruvA | CH53_167 | CH53_3801 | ftsK/SpoIIIE family protein. | Holliday junction DNA helicase RuvA; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB. | 0.479 |
| guaA | ftsK | CH53_620 | CH53_167 | GMP synthase; Catalyzes the synthesis of GMP from XMP. | ftsK/SpoIIIE family protein. | 0.423 |
| guaA | nadE | CH53_620 | CH53_663 | GMP synthase; Catalyzes the synthesis of GMP from XMP. | NAD+ synthetase; Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source. | 0.624 |
| guaA | polA | CH53_620 | CH53_1803 | GMP synthase; Catalyzes the synthesis of GMP from XMP. | Pola: DNA polymerase I. | 0.664 |
| guaA | rarA | CH53_620 | CH53_165 | GMP synthase; Catalyzes the synthesis of GMP from XMP. | Replication-associated recombination protein A. | 0.460 |
| guaA | serS | CH53_620 | CH53_164 | GMP synthase; Catalyzes the synthesis of GMP from XMP. | serine--tRNA ligase; Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L- seryl-tRNA(Sec), which will be further converted into selenocysteinyl- tRNA(Sec). | 0.608 |
| lolA | ftsK | CH53_166 | CH53_167 | Outer membrane lipocarrier protein LolA; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | ftsK/SpoIIIE family protein. | 0.829 |
| lolA | rarA | CH53_166 | CH53_165 | Outer membrane lipocarrier protein LolA; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | Replication-associated recombination protein A. | 0.832 |
| lolA | serS | CH53_166 | CH53_164 | Outer membrane lipocarrier protein LolA; Participates in the translocation of lipoproteins from the inner membrane to the outer membrane. Only forms a complex with a lipoprotein if the residue after the N-terminal Cys is not an aspartate (The Asp acts as a targeting signal to indicate that the lipoprotein should stay in the inner membrane). | serine--tRNA ligase; Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L- seryl-tRNA(Sec), which will be further converted into selenocysteinyl- tRNA(Sec). | 0.664 |
| nadE | guaA | CH53_663 | CH53_620 | NAD+ synthetase; Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source. | GMP synthase; Catalyzes the synthesis of GMP from XMP. | 0.624 |
| nadE | rarA | CH53_663 | CH53_165 | NAD+ synthetase; Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source. | Replication-associated recombination protein A. | 0.552 |
| ogt | dinB | CH53_4022 | CH53_2798 | methylated-DNA--protein-cysteine methyltransferase; Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction: the enzyme is irreversibly inactivated. | 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. | 0.423 |