| 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. | 0.807 |
| 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. | 0.784 |
| 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. | 0.772 |
| 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. | 0.807 |
| 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. | 0.471 |
| 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. | 0.768 |
| 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. | 0.904 |
| 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. | 0.471 |
| 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. | 0.767 |
| AMP24797.1 | xerC | VC42_21260 | VC42_23115 | Quinone oxidoreductase; 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. | 0.740 |
| 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. | 0.766 |
| 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. | 0.765 |
| 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. | 0.784 |
| 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. | 0.768 |
| 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. | 0.766 |
| 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. | 0.864 |
| rbpA | whiA | VC42_03050 | VC42_25445 | Membrane protein; Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters. Belongs to the RNA polymerase-binding protein RbpA family. | Sporulation protein; Involved in cell division and chromosome segregation. | 0.759 |
| rbpA | xerC | VC42_03050 | VC42_23115 | Membrane protein; Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters. Belongs to the RNA polymerase-binding protein RbpA 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. | 0.817 |
| sucC | sucD | VC42_09520 | VC42_09515 | succinyl-CoA synthetase subunit beta; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit. | succinyl-CoA synthetase subunit alpha; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit. | 0.999 |
| sucC | xerC | VC42_09520 | VC42_23115 | succinyl-CoA synthetase subunit beta; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit. | 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. | 0.740 |
STRING v12.5 is now available!
