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 |
| ADAMTS13 | F10 | ENSSSCP00000074476 | ENSSSCP00000010205 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Uncharacterized protein. | 0.512 |
| ADAMTS13 | F8 | ENSSSCP00000074476 | ENSSSCP00000028556 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Coagulation factor VIII; Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. | 0.568 |
| ADAMTS13 | VWF | ENSSSCP00000074476 | ENSSSCP00000000759 | ADAM metallopeptidase with thrombospondin type 1 motif 13. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.938 |
| ATP7A | F8 | ENSSSCP00000013235 | ENSSSCP00000028556 | ATPase copper transporting alpha. | Coagulation factor VIII; Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. | 0.534 |
| ATP7A | VWF | ENSSSCP00000013235 | ENSSSCP00000000759 | ATPase copper transporting alpha. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.574 |
| CLEC1B | F8 | ENSSSCP00000025784 | ENSSSCP00000028556 | C-type lectin domain family 1 member B. | Coagulation factor VIII; Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. | 0.581 |
| F10 | ADAMTS13 | ENSSSCP00000010205 | ENSSSCP00000074476 | Uncharacterized protein. | ADAM metallopeptidase with thrombospondin type 1 motif 13. | 0.512 |
| F10 | F2 | ENSSSCP00000010205 | ENSSSCP00000014081 | Uncharacterized protein. | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | 0.975 |
| F10 | F7 | ENSSSCP00000010205 | ENSSSCP00000010206 | Uncharacterized protein. | Uncharacterized protein. | 0.955 |
| F10 | F8 | ENSSSCP00000010205 | ENSSSCP00000028556 | Uncharacterized protein. | Coagulation factor VIII; Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. | 0.609 |
| F10 | F9 | ENSSSCP00000010205 | ENSSSCP00000013514 | Uncharacterized protein. | Coagulation factor IXa heavy chain; Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca(2+) ions, phospholipids, and factor VIIIa. | 0.910 |
| F10 | SERPINC1 | ENSSSCP00000010205 | ENSSSCP00000067774 | Uncharacterized protein. | SERPIN domain-containing protein; Belongs to the serpin family. | 0.986 |
| F10 | VWF | ENSSSCP00000010205 | ENSSSCP00000000759 | Uncharacterized protein. | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.933 |
| F2 | F10 | ENSSSCP00000014081 | ENSSSCP00000010205 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Uncharacterized protein. | 0.975 |
| F2 | F7 | ENSSSCP00000014081 | ENSSSCP00000010206 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Uncharacterized protein. | 0.653 |
| F2 | F8 | ENSSSCP00000014081 | ENSSSCP00000028556 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Coagulation factor VIII; Factor VIII, along with calcium and phospholipid, acts as a cofactor for factor IXa when it converts factor X to the activated form, factor Xa. | 0.840 |
| F2 | F9 | ENSSSCP00000014081 | ENSSSCP00000013514 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Coagulation factor IXa heavy chain; Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca(2+) ions, phospholipids, and factor VIIIa. | 0.837 |
| F2 | FN1 | ENSSSCP00000014081 | ENSSSCP00000017132 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Fibronectin 1. | 0.553 |
| F2 | SERPINC1 | ENSSSCP00000014081 | ENSSSCP00000067774 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | SERPIN domain-containing protein; Belongs to the serpin family. | 0.999 |
| F2 | VWF | ENSSSCP00000014081 | ENSSSCP00000000759 | Activation peptide fragment 1; Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing (By similarity). | Von Willebrand factor; Important in the maintenance of hemostasis, it promotes adhesion of platelets to the sites of vascular injury by forming a molecular bridge between sub-endothelial collagen matrix and platelet- surface receptor complex, glycoprotein Ibalpha/IX/V. Also acts as a chaperone for coagulation factor VIII, delivering it to the site of injury, stabilizing its heterodimeric structure and protecting it from premature clearance from plasma (By similarity). | 0.882 |
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