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 |
| A0A1L9WER6 | A0A1L9WK64 | A0A1L9WER6 | A0A1L9WK64 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | E2_bind domain-containing protein. | 0.798 |
| A0A1L9WER6 | A0A1L9WLQ8 | A0A1L9WER6 | A0A1L9WLQ8 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | UBA_e1_C domain-containing protein; Belongs to the ubiquitin-activating E1 family. | 0.826 |
| A0A1L9WER6 | A0A1L9WNS3 | A0A1L9WER6 | A0A1L9WNS3 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | UBIQUITIN_CONJUGAT_2 domain-containing protein. | 0.702 |
| A0A1L9WER6 | A0A1L9WRI2 | A0A1L9WER6 | A0A1L9WRI2 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | ATP_bind_3 domain-containing protein. | 0.426 |
| A0A1L9WER6 | A0A1L9WUI5 | A0A1L9WER6 | A0A1L9WUI5 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | ThiF domain-containing protein. | 0.681 |
| A0A1L9WER6 | uba4 | A0A1L9WER6 | A0A1L9WZ82 | Ubiquitin-like modifier-activating enzyme ATG7; E1-like activating enzyme involved in the 2 ubiquitin-like systems required for cytoplasm to vacuole transport (Cvt) and autophagy. Activates ATG12 for its conjugation with ATG5 and ATG8 for its conjugation with phosphatidylethanolamine. Both systems are needed for the ATG8 association to Cvt vesicles and autophagosomes membranes. Autophagy is essential for maintenance of amino acid levels and protein synthesis under nitrogen starvation. Required for selective autophagic degradation of the nucleus (nucleophagy) as well as for mitophagy wh [...] | Adenylyltransferase and sulfurtransferase uba4; Plays a central role in 2-thiolation of mcm(5)S(2)U at tRNA wobble positions of cytosolic tRNA(Lys), tRNA(Glu) and tRNA(Gln). Also essential during biosynthesis of the molybdenum cofactor. Acts by mediating the C-terminal thiocarboxylation of sulfur carriers urm1 and MOCS2A. Its N-terminus first activates urm1 and MOCS2A as acyl- adenylates (-COAMP), then the persulfide sulfur on the catalytic cysteine is transferred to urm1 and MOCS2A to form thiocarboxylation (- COSH) of their C-terminus. The reaction probably involves hydrogen sulfide [...] | 0.447 |
| A0A1L9WEU1 | A0A1L9WGF0 | A0A1L9WEU1 | A0A1L9WGF0 | Uncharacterized protein. | Uncharacterized protein. | 0.747 |
| A0A1L9WEU1 | A0A1L9WGG3 | A0A1L9WEU1 | A0A1L9WGG3 | Uncharacterized protein. | Uncharacterized protein. | 0.976 |
| A0A1L9WEU1 | A0A1L9WIB8 | A0A1L9WEU1 | A0A1L9WIB8 | Uncharacterized protein. | Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of ATP 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. | 0.737 |
| A0A1L9WEU1 | A0A1L9WKU7 | A0A1L9WEU1 | A0A1L9WKU7 | Uncharacterized protein. | Succinate--CoA ligase [ADP-forming] subunit alpha, mitochondrial; Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of ATP 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. | 0.634 |
| A0A1L9WEU1 | A0A1L9WMM0 | A0A1L9WEU1 | A0A1L9WMM0 | Uncharacterized protein. | Uncharacterized protein. | 0.553 |
| A0A1L9WEU1 | A0A1L9WMQ4 | A0A1L9WEU1 | A0A1L9WMQ4 | Uncharacterized protein. | Uncharacterized protein. | 0.662 |
| A0A1L9WEU1 | A0A1L9WMW0 | A0A1L9WEU1 | A0A1L9WMW0 | Uncharacterized protein. | Uncharacterized protein. | 0.441 |
| A0A1L9WEU1 | A0A1L9WP60 | A0A1L9WEU1 | A0A1L9WP60 | Uncharacterized protein. | Glutamine synthetase. | 0.530 |
| A0A1L9WEU1 | A0A1L9WRS9 | A0A1L9WEU1 | A0A1L9WRS9 | Uncharacterized protein. | Glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial; Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in the mitochondria. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln). Belongs to the amidase family. GatA subfamily. | 0.497 |
| A0A1L9WEU1 | A0A1L9WSE0 | A0A1L9WEU1 | A0A1L9WSE0 | Uncharacterized protein. | Uncharacterized protein. | 0.499 |
| A0A1L9WEU1 | A0A1L9WU23 | A0A1L9WEU1 | A0A1L9WU23 | Uncharacterized protein. | Uncharacterized protein. | 0.975 |
| A0A1L9WEU1 | A0A1L9WWF4 | A0A1L9WEU1 | A0A1L9WWF4 | Uncharacterized protein. | Uncharacterized protein. | 0.499 |
| A0A1L9WEU1 | A0A1L9WWH0 | A0A1L9WEU1 | A0A1L9WWH0 | Uncharacterized protein. | Uncharacterized protein. | 0.703 |
| A0A1L9WEU1 | A0A1L9WWN4 | A0A1L9WEU1 | A0A1L9WWN4 | Uncharacterized protein. | CoA_binding domain-containing protein. | 0.628 |
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