| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| PSHAa0024 | PSHAa0027 | PSHAa0024 | PSHAa0027 | Homologs of previously reported genes of unknown function. | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | 0.613 |
| PSHAa0024 | def | PSHAa0024 | PSHAa0023 | Homologs of previously reported genes of unknown function. | N-terminal methionine peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | 0.603 |
| PSHAa0024 | fmt | PSHAa0024 | PSHAa0022 | Homologs of previously reported genes of unknown function. | 10-formyltetrahydrofolate:L-methionyl-tRNA(fMet) N-formyltransferase; Attaches a formyl group to the free amino group of methionyl- tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus; Belongs to the Fmt family. | 0.727 |
| PSHAa0024 | hemF | PSHAa0024 | PSHAa0029 | Homologs of previously reported genes of unknown function. | Coproporphyrinogen III oxidase; Involved in the heme biosynthesis. Catalyzes the aerobic oxidative decarboxylation of propionate groups of rings A and B of coproporphyrinogen-III to yield the vinyl groups in protoporphyrinogen- IX. | 0.606 |
| PSHAa0024 | rsmB | PSHAa0024 | PSHAa0021 | Homologs of previously reported genes of unknown function. | 16S rRNA m5C967 methyltransferase, S-adenosyl-L-methionine-dependent; Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA. | 0.727 |
| PSHAa0024 | smf | PSHAa0024 | PSHAa0025 | Homologs of previously reported genes of unknown function. | Homologs of previously reported genes of unknown function. | 0.825 |
| PSHAa0024 | smg | PSHAa0024 | PSHAa0026 | Homologs of previously reported genes of unknown function. | Homologs of previously reported genes of unknown function; Belongs to the Smg family. | 0.730 |
| PSHAa0024 | tsaC | PSHAa0024 | PSHAa0028 | Homologs of previously reported genes of unknown function. | Putative double-stranded RNA-binding protein with unique protein fold, with YrdC/RibB domain; Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Catalyzes the conversion of L-threonine, HCO(3)(-)/CO(2) and ATP to give threonylcarbamoyl-AMP (TC-AMP) as the acyladenylate intermediate, with the release of diphosphate. | 0.606 |
| PSHAa0027 | PSHAa0024 | PSHAa0027 | PSHAa0024 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Homologs of previously reported genes of unknown function. | 0.613 |
| PSHAa0027 | def | PSHAa0027 | PSHAa0023 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | N-terminal methionine peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | 0.604 |
| PSHAa0027 | fmt | PSHAa0027 | PSHAa0022 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | 10-formyltetrahydrofolate:L-methionyl-tRNA(fMet) N-formyltransferase; Attaches a formyl group to the free amino group of methionyl- tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus; Belongs to the Fmt family. | 0.617 |
| PSHAa0027 | hemF | PSHAa0027 | PSHAa0029 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Coproporphyrinogen III oxidase; Involved in the heme biosynthesis. Catalyzes the aerobic oxidative decarboxylation of propionate groups of rings A and B of coproporphyrinogen-III to yield the vinyl groups in protoporphyrinogen- IX. | 0.832 |
| PSHAa0027 | rsmB | PSHAa0027 | PSHAa0021 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | 16S rRNA m5C967 methyltransferase, S-adenosyl-L-methionine-dependent; Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA. | 0.589 |
| PSHAa0027 | smf | PSHAa0027 | PSHAa0025 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Homologs of previously reported genes of unknown function. | 0.763 |
| PSHAa0027 | smg | PSHAa0027 | PSHAa0026 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Homologs of previously reported genes of unknown function; Belongs to the Smg family. | 0.788 |
| PSHAa0027 | ssb | PSHAa0027 | PSHAa2705 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Single-strand binding protein (SSB) (Helix-destabilizing protein); Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism. | 0.444 |
| PSHAa0027 | tsaC | PSHAa0027 | PSHAa0028 | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | Putative double-stranded RNA-binding protein with unique protein fold, with YrdC/RibB domain; Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Catalyzes the conversion of L-threonine, HCO(3)(-)/CO(2) and ATP to give threonylcarbamoyl-AMP (TC-AMP) as the acyladenylate intermediate, with the release of diphosphate. | 0.941 |
| def | PSHAa0024 | PSHAa0023 | PSHAa0024 | N-terminal methionine peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | Homologs of previously reported genes of unknown function. | 0.603 |
| def | PSHAa0027 | PSHAa0023 | PSHAa0027 | N-terminal methionine peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | Putative DNA topoisomerase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homolgy; enzyme. | 0.604 |
| def | fmt | PSHAa0023 | PSHAa0022 | N-terminal methionine peptide deformylase; Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions. | 10-formyltetrahydrofolate:L-methionyl-tRNA(fMet) N-formyltransferase; Attaches a formyl group to the free amino group of methionyl- tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus; Belongs to the Fmt family. | 0.992 |