| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| THA_1676 | THA_586 | THA_1676 | THA_586 | Lipopolysaccharide biosynthesis protein, putative; Belongs to the glycosyltransferase 26 family. | Membrane protein, putative. | 0.784 |
| THA_1676 | THA_902 | THA_1676 | THA_902 | Lipopolysaccharide biosynthesis protein, putative; Belongs to the glycosyltransferase 26 family. | Methicillin resistance protein. | 0.766 |
| THA_586 | THA_1676 | THA_586 | THA_1676 | Membrane protein, putative. | Lipopolysaccharide biosynthesis protein, putative; Belongs to the glycosyltransferase 26 family. | 0.784 |
| THA_586 | THA_587 | THA_586 | THA_587 | Membrane protein, putative. | Conserved hypothetical protein. | 0.779 |
| THA_586 | THA_590 | THA_586 | THA_590 | Membrane protein, putative. | Pleiotropic regulatory protein; Belongs to the DegT/DnrJ/EryC1 family. | 0.632 |
| THA_586 | THA_591 | THA_586 | THA_591 | Membrane protein, putative. | Conserved hypothetical protein. | 0.576 |
| THA_586 | THA_790 | THA_586 | THA_790 | Membrane protein, putative. | UDP-N-acetylmuramyl pentapeptide synthase. | 0.707 |
| THA_586 | THA_902 | THA_586 | THA_902 | Membrane protein, putative. | Methicillin resistance protein. | 0.973 |
| THA_586 | metG | THA_586 | THA_1573 | Membrane protein, putative. | methionyl-tRNA synthetase; Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation. | 0.535 |
| THA_586 | murD | THA_586 | THA_468 | Membrane protein, putative. | UDP-N-acetylmuramoylalanine--D-glutamate ligase; Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA). Belongs to the MurCDEF family. | 0.726 |
| THA_586 | nth | THA_586 | THA_589 | Membrane protein, putative. | Nth endonuclease III; DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N-glycosidic bond, leaving an AP (apurinic/apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'- phosphate. | 0.576 |
| THA_586 | ribF | THA_586 | THA_588 | Membrane protein, putative. | Riboflavin biosynthesis protein RibF; Belongs to the ribF family. | 0.588 |
| THA_587 | THA_586 | THA_587 | THA_586 | Conserved hypothetical protein. | Membrane protein, putative. | 0.779 |
| THA_587 | THA_590 | THA_587 | THA_590 | Conserved hypothetical protein. | Pleiotropic regulatory protein; Belongs to the DegT/DnrJ/EryC1 family. | 0.595 |
| THA_587 | THA_591 | THA_587 | THA_591 | Conserved hypothetical protein. | Conserved hypothetical protein. | 0.576 |
| THA_587 | nth | THA_587 | THA_589 | Conserved hypothetical protein. | Nth endonuclease III; DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N-glycosidic bond, leaving an AP (apurinic/apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'- phosphate. | 0.576 |
| THA_587 | ribF | THA_587 | THA_588 | Conserved hypothetical protein. | Riboflavin biosynthesis protein RibF; Belongs to the ribF family. | 0.598 |
| THA_590 | THA_586 | THA_590 | THA_586 | Pleiotropic regulatory protein; Belongs to the DegT/DnrJ/EryC1 family. | Membrane protein, putative. | 0.632 |
| THA_590 | THA_587 | THA_590 | THA_587 | Pleiotropic regulatory protein; Belongs to the DegT/DnrJ/EryC1 family. | Conserved hypothetical protein. | 0.595 |
| THA_590 | THA_591 | THA_590 | THA_591 | Pleiotropic regulatory protein; Belongs to the DegT/DnrJ/EryC1 family. | Conserved hypothetical protein. | 0.807 |