| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| AMP23575.1 | AMP24654.1 | VC42_13510 | VC42_20350 | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.836 |
| AMP23575.1 | apt | VC42_13510 | VC42_24870 | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | 0.839 |
| AMP23575.1 | murG | VC42_13510 | VC42_03730 | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Hypothetical protein; Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II); Belongs to the glycosyltransferase 28 family. MurG subfamily. | 0.400 |
| AMP23575.1 | xerC | VC42_13510 | VC42_23115 | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.805 |
| AMP24130.1 | xerC | VC42_17060 | VC42_23115 | Hypothetical protein; Derived by automated computational analysis using gene prediction method: Protein Homology. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.707 |
| AMP24654.1 | AMP23575.1 | VC42_20350 | VC42_13510 | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.836 |
| AMP24654.1 | AMP24668.1 | VC42_20350 | VC42_20445 | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Bacteriophage protein; Derived by automated computational analysis using gene prediction method: Protein Homology; Belongs to the SOS response-associated peptidase family. | 0.456 |
| AMP24654.1 | apt | VC42_20350 | VC42_24870 | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | 0.839 |
| AMP24654.1 | xerC | VC42_20350 | VC42_23115 | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.842 |
| AMP24668.1 | AMP24654.1 | VC42_20445 | VC42_20350 | Bacteriophage protein; Derived by automated computational analysis using gene prediction method: Protein Homology; Belongs to the SOS response-associated peptidase family. | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.456 |
| AMP24668.1 | xerC | VC42_20445 | VC42_23115 | Bacteriophage protein; Derived by automated computational analysis using gene prediction method: Protein Homology; Belongs to the SOS response-associated peptidase family. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.799 |
| AMP26410.1 | apt | VC42_23465 | VC42_24870 | Histidine kinase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | 0.814 |
| AMP26410.1 | xerC | VC42_23465 | VC42_23115 | Histidine kinase; Derived by automated computational analysis using gene prediction method: Protein Homology. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.797 |
| AMP26430.1 | murG | VC42_23995 | VC42_03730 | Cell division protein FtsK; Derived by automated computational analysis using gene prediction method: Protein Homology. | Hypothetical protein; Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II); Belongs to the glycosyltransferase 28 family. MurG subfamily. | 0.434 |
| AMP26430.1 | whiA | VC42_23995 | VC42_25445 | Cell division protein FtsK; Derived by automated computational analysis using gene prediction method: Protein Homology. | Sporulation protein; Involved in cell division and chromosome segregation. | 0.440 |
| AMP26430.1 | xerC | VC42_23995 | VC42_23115 | Cell division protein FtsK; Derived by automated computational analysis using gene prediction method: Protein Homology. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.712 |
| apt | AMP23575.1 | VC42_24870 | VC42_13510 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Prephenate dehydrogenase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.839 |
| apt | AMP24654.1 | VC42_24870 | VC42_20350 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Phosphoribosyltransferase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.839 |
| apt | AMP26410.1 | VC42_24870 | VC42_23465 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Histidine kinase; Derived by automated computational analysis using gene prediction method: Protein Homology. | 0.814 |
| apt | xerC | VC42_24870 | VC42_23115 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Recombinase XerC; Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. The XerC- XerD complex is essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division. It also contributes to the segregational stability of plasmids. | 0.840 |
