Export your current network:
... as a vector graphic:
SVG: scalable vector graphic - can be opened and edited in Illustrator, CorelDraw, Dia, etc
... as short tabular text output:
TSV: tab separated values - can be opened in Excel and Cytoscape (lists only one-way edges: A-B)
... as tabular text output:
TSV: tab separated values - can be opened in Excel (lists reciprocal edges: A-B,B-A)
... as an XML summary:
structured XML interaction data, according to the 'PSI-MI' data standard
... protein node degrees:
node degree of proteins in your network (given the current score cut-off)
... network coordinates:
a flat-file format describing the coordinates and colors of nodes in the network
... protein sequences:
MFA: multi-fasta format - containing the aminoacid sequences in the network
... protein annotations:
a tab-delimited file describing the names, domains and descriptions of proteins in your network
... functional annotations:
a tab-delimited file containing all known functional terms of protiens in your network
Browse interactions in tabular form:
| node1 | node2 | node1 accession | node2 accession | node1 annotation | node2 annotation | score |
| SED65173.1 | SEE04294.1 | SAMN04488554_0351 | SAMN04488554_1378 | Phosphotransacetylase; Involved in acetate metabolism. In the N-terminal section; belongs to the CobB/CobQ family. | 3-hydroxyacyl-CoA dehydrogenase. | 0.977 |
| SED65173.1 | sucC | SAMN04488554_0351 | SAMN04488554_0369 | Phosphotransacetylase; Involved in acetate metabolism. In the N-terminal section; belongs to the CobB/CobQ family. | succinyl-CoA synthetase (ADP-forming) beta subunit; 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. | 0.935 |
| SED65173.1 | sucD | SAMN04488554_0351 | SAMN04488554_0370 | Phosphotransacetylase; Involved in acetate metabolism. In the N-terminal section; belongs to the CobB/CobQ family. | succinyl-CoA synthetase (ADP-forming) alpha subunit; 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. | 0.941 |
| SED65173.1 | xerC | SAMN04488554_0351 | SAMN04488554_0858 | Phosphotransacetylase; Involved in acetate metabolism. In the N-terminal section; belongs to the CobB/CobQ family. | Integrase/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. | 0.829 |
| SED72796.1 | xerC | SAMN04488554_0541 | SAMN04488554_0858 | Putative SOS response-associated peptidase YedK; Belongs to the SOS response-associated peptidase family. | Integrase/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. | 0.703 |
| SED86123.1 | whiA | SAMN04488554_0893 | SAMN04488554_1630 | DNA segregation ATPase FtsK/SpoIIIE, S-DNA-T family. | Hypothetical protein; Involved in cell division and chromosome segregation. | 0.434 |
| SED86123.1 | xerC | SAMN04488554_0893 | SAMN04488554_0858 | DNA segregation ATPase FtsK/SpoIIIE, S-DNA-T family. | Integrase/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. | 0.780 |
| SEE04294.1 | SED65173.1 | SAMN04488554_1378 | SAMN04488554_0351 | 3-hydroxyacyl-CoA dehydrogenase. | Phosphotransacetylase; Involved in acetate metabolism. In the N-terminal section; belongs to the CobB/CobQ family. | 0.977 |
| SEE04294.1 | sucC | SAMN04488554_1378 | SAMN04488554_0369 | 3-hydroxyacyl-CoA dehydrogenase. | succinyl-CoA synthetase (ADP-forming) beta subunit; 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. | 0.571 |
| SEE04294.1 | sucD | SAMN04488554_1378 | SAMN04488554_0370 | 3-hydroxyacyl-CoA dehydrogenase. | succinyl-CoA synthetase (ADP-forming) alpha subunit; 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. | 0.548 |
| SEE04294.1 | xerC | SAMN04488554_1378 | SAMN04488554_0858 | 3-hydroxyacyl-CoA dehydrogenase. | Integrase/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. | 0.804 |
| SEE13342.1 | SEE98935.1 | SAMN04488554_1608 | SAMN04488554_4161 | Prephenate dehydrogenase. | Predicted amidophosphoribosyltransferases. | 0.753 |
| SEE13342.1 | apt | SAMN04488554_1608 | SAMN04488554_1413 | Prephenate dehydrogenase. | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | 0.739 |
| SEE13342.1 | xerC | SAMN04488554_1608 | SAMN04488554_0858 | Prephenate dehydrogenase. | Integrase/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. | 0.718 |
| SEE98935.1 | SEE13342.1 | SAMN04488554_4161 | SAMN04488554_1608 | Predicted amidophosphoribosyltransferases. | Prephenate dehydrogenase. | 0.753 |
| SEE98935.1 | apt | SAMN04488554_4161 | SAMN04488554_1413 | Predicted amidophosphoribosyltransferases. | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | 0.731 |
| SEE98935.1 | xerC | SAMN04488554_4161 | SAMN04488554_0858 | Predicted amidophosphoribosyltransferases. | Integrase/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. | 0.812 |
| apt | SEE13342.1 | SAMN04488554_1413 | SAMN04488554_1608 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Prephenate dehydrogenase. | 0.739 |
| apt | SEE98935.1 | SAMN04488554_1413 | SAMN04488554_4161 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Predicted amidophosphoribosyltransferases. | 0.731 |
| apt | xerC | SAMN04488554_1413 | SAMN04488554_0858 | Adenine phosphoribosyltransferase; Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis. | Integrase/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. | 0.753 |
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