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 |
| Renbp | nagZ | ING2E5A_0837 | ING2E5A_1767 | N-acylglucosamine 2-epimerase; Catalyzes the interconversion of N-acetylglucosamine to N-acetylmannosamine. Binds to renin forming a protein complex called high molecular weight (HMW) renin and inhibits renin activity. Involved in the N-glycolylneuraminic acid (Neu5Gc) degradation pathway. Event=Alternative splicing; Named isoforms=2; Name=1; IsoId=P82343-1; Name=2; IsoId=P82343-2; Sequence=VSP_039024; the initiator. Sequence=AAH14821.1; Type=Erroneous initiation; Note=Translation N-terminally extended; Evidence=; Sequence=AAO66340.1; Type=Erroneous initiation; Note=Translation N-termi [...] | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.900 |
| SCM55203.1 | SCM55278.1 | ING2E5A_0118 | ING2E5A_0198 | Putative membrane protein {ECO:0000313|EMBL:CEA14712,1}; tr|A0A098BYY0|A0A098BYY0_9PORP;evalue=2e-092; PctID=50.75; score=345. | Putative protein {ECO:0000313|EMBL:CEA16579,1}; tr|A0A098C0W6|A0A098C0W6_9PORP;evalue=7e-100; PctID=61.36; score=370. | 0.538 |
| SCM55203.1 | SCM56767.1 | ING2E5A_0118 | ING2E5A_1038 | Putative membrane protein {ECO:0000313|EMBL:CEA14712,1}; tr|A0A098BYY0|A0A098BYY0_9PORP;evalue=2e-092; PctID=50.75; score=345. | Putative protein {ECO:0000313|EMBL:CEA16321,1}; tr|A0A098C1M9|A0A098C1M9_9PORP;evalue=5e-032; PctID=56.56; score=142. | 0.552 |
| SCM55203.1 | nagZ | ING2E5A_0118 | ING2E5A_1767 | Putative membrane protein {ECO:0000313|EMBL:CEA14712,1}; tr|A0A098BYY0|A0A098BYY0_9PORP;evalue=2e-092; PctID=50.75; score=345. | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.677 |
| SCM55278.1 | SCM55203.1 | ING2E5A_0198 | ING2E5A_0118 | Putative protein {ECO:0000313|EMBL:CEA16579,1}; tr|A0A098C0W6|A0A098C0W6_9PORP;evalue=7e-100; PctID=61.36; score=370. | Putative membrane protein {ECO:0000313|EMBL:CEA14712,1}; tr|A0A098BYY0|A0A098BYY0_9PORP;evalue=2e-092; PctID=50.75; score=345. | 0.538 |
| SCM55278.1 | SCM56767.1 | ING2E5A_0198 | ING2E5A_1038 | Putative protein {ECO:0000313|EMBL:CEA16579,1}; tr|A0A098C0W6|A0A098C0W6_9PORP;evalue=7e-100; PctID=61.36; score=370. | Putative protein {ECO:0000313|EMBL:CEA16321,1}; tr|A0A098C1M9|A0A098C1M9_9PORP;evalue=5e-032; PctID=56.56; score=142. | 0.460 |
| SCM55278.1 | nagZ | ING2E5A_0198 | ING2E5A_1767 | Putative protein {ECO:0000313|EMBL:CEA16579,1}; tr|A0A098C0W6|A0A098C0W6_9PORP;evalue=7e-100; PctID=61.36; score=370. | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.614 |
| SCM56767.1 | SCM55203.1 | ING2E5A_1038 | ING2E5A_0118 | Putative protein {ECO:0000313|EMBL:CEA16321,1}; tr|A0A098C1M9|A0A098C1M9_9PORP;evalue=5e-032; PctID=56.56; score=142. | Putative membrane protein {ECO:0000313|EMBL:CEA14712,1}; tr|A0A098BYY0|A0A098BYY0_9PORP;evalue=2e-092; PctID=50.75; score=345. | 0.552 |
| SCM56767.1 | SCM55278.1 | ING2E5A_1038 | ING2E5A_0198 | Putative protein {ECO:0000313|EMBL:CEA16321,1}; tr|A0A098C1M9|A0A098C1M9_9PORP;evalue=5e-032; PctID=56.56; score=142. | Putative protein {ECO:0000313|EMBL:CEA16579,1}; tr|A0A098C0W6|A0A098C0W6_9PORP;evalue=7e-100; PctID=61.36; score=370. | 0.460 |
| SCM56767.1 | nagZ | ING2E5A_1038 | ING2E5A_1767 | Putative protein {ECO:0000313|EMBL:CEA16321,1}; tr|A0A098C1M9|A0A098C1M9_9PORP;evalue=5e-032; PctID=56.56; score=142. | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.514 |
| SCM58338.1 | SCM58340.1 | ING2E5A_1765 | ING2E5A_1766 | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | 0.994 |
| SCM58338.1 | aroB | ING2E5A_1765 | ING2E5A_1768 | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | 3-dehydroquinate synthase {ECO:0000255|HAMAP-Rule:MF_00110}; Catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ). | 0.741 |
| SCM58338.1 | nagZ | ING2E5A_1765 | ING2E5A_1767 | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.767 |
| SCM58338.1 | rplS | ING2E5A_1765 | ING2E5A_1764 | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | 50S ribosomal protein L19 {ECO:0000255|HAMAP-Rule:MF_00402}; This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site. | 0.536 |
| SCM58340.1 | SCM58338.1 | ING2E5A_1766 | ING2E5A_1765 | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | 0.994 |
| SCM58340.1 | aroB | ING2E5A_1766 | ING2E5A_1768 | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | 3-dehydroquinate synthase {ECO:0000255|HAMAP-Rule:MF_00110}; Catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ). | 0.773 |
| SCM58340.1 | nagZ | ING2E5A_1766 | ING2E5A_1767 | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | Beta-hexosaminidase; Plays a role in peptidoglycan recycling by cleaving the terminal beta-1,4-linked N-acetylglucosamine (GlcNAc) from peptide-linked peptidoglycan fragments, giving rise to free GlcNAc, anhydro-N-acetylmuramic acid and anhydro-N-acetylmuramic acid-linked peptides. Cleaves muropeptides, but not peptidoglycan. D-hexosamine residues in N-acetyl-beta-D-hexosaminides. pH dependence: Optimum pH is 5.8-6.2; ProRule:PRU00303}; Lipid-anchor Secreted, cell wall Note=Detected in the culture supernatant, predominantly associated with cell wall-derived particulate material. A mino [...] | 0.796 |
| SCM58340.1 | rplS | ING2E5A_1766 | ING2E5A_1764 | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | 50S ribosomal protein L19 {ECO:0000255|HAMAP-Rule:MF_00402}; This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site. | 0.497 |
| aroB | SCM58338.1 | ING2E5A_1768 | ING2E5A_1765 | 3-dehydroquinate synthase {ECO:0000255|HAMAP-Rule:MF_00110}; Catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ). | Putative protein {ECO:0000313|EMBL:CEA16483,1}; tr|A0A098C250|A0A098C250_9PORP;evalue=2e-087; PctID=65.74; score=328. | 0.741 |
| aroB | SCM58340.1 | ING2E5A_1768 | ING2E5A_1766 | 3-dehydroquinate synthase {ECO:0000255|HAMAP-Rule:MF_00110}; Catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ). | Snake venom 5'-nucleotidase; Hydrolyzes nucleotides into nucleosides (By similarity). Snake venom 5'-nucleotidases are widely distributed among venomous snake taxa, but there is a lack of information about their biological activities. They have been shown to inhibit platelet aggregation. This effect may be due to the liberation of inhibitory AMP or adenosine by its action on ADP released upon initiation of aggregation. Venom 5'-nucleotidases are also known to synergistically act in vivo with other toxins like ADPases, phospholipases, and disintegrins to exert a more pronounced anti-coa [...] | 0.773 |
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