Export your current network:
... as a bitmap image:
file format is 'PNG': portable network graphic
... as a high-resolution bitmap:
same PNG format, but at higher resolution
... 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 |
ALDH16A1 | PAAF1 | ENSEASP00005006775 | ENSEASP00005026280 | Aldehyde dehydrogenase 16 family member A1. | Proteasomal ATPase associated factor 1. | 0.634 |
ALDH16A1 | SPG21 | ENSEASP00005006775 | ENSEASP00005009087 | Aldehyde dehydrogenase 16 family member A1. | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.594 |
ENSEASP00005008844 | GPC3 | ENSEASP00005008844 | ENSEASP00005027138 | annotation not available | Glypican 3. | 0.692 |
ENSEASP00005008844 | LTF | ENSEASP00005008844 | ENSEASP00005011514 | annotation not available | Lactotransferrin. | 0.691 |
ENSEASP00005008844 | SPG21 | ENSEASP00005008844 | ENSEASP00005009087 | annotation not available | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.735 |
ENSEASP00005008844 | TNFSF15 | ENSEASP00005008844 | ENSEASP00005033075 | annotation not available | TNF superfamily member 15. | 0.733 |
GPC3 | ENSEASP00005008844 | ENSEASP00005027138 | ENSEASP00005008844 | Glypican 3. | annotation not available | 0.692 |
GPC3 | LTF | ENSEASP00005027138 | ENSEASP00005011514 | Glypican 3. | Lactotransferrin. | 0.507 |
GPC3 | SPG21 | ENSEASP00005027138 | ENSEASP00005009087 | Glypican 3. | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.692 |
GPC3 | TNFSF15 | ENSEASP00005027138 | ENSEASP00005033075 | Glypican 3. | TNF superfamily member 15. | 0.692 |
LTF | ENSEASP00005008844 | ENSEASP00005011514 | ENSEASP00005008844 | Lactotransferrin. | annotation not available | 0.691 |
LTF | GPC3 | ENSEASP00005011514 | ENSEASP00005027138 | Lactotransferrin. | Glypican 3. | 0.507 |
LTF | SPG21 | ENSEASP00005011514 | ENSEASP00005009087 | Lactotransferrin. | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.666 |
LTF | TNFSF15 | ENSEASP00005011514 | ENSEASP00005033075 | Lactotransferrin. | TNF superfamily member 15. | 0.690 |
NIPA1 | SPG11 | ENSEASP00005030692 | ENSEASP00005026397 | Non imprinted in Prader-Willi/Angelman syndrome 1. | Spastic paraplegia 11 (autosomal recessive). | 0.711 |
NIPA1 | SPG21 | ENSEASP00005030692 | ENSEASP00005009087 | Non imprinted in Prader-Willi/Angelman syndrome 1. | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.592 |
NIPA1 | SPG7 | ENSEASP00005030692 | ENSEASP00005001035 | Non imprinted in Prader-Willi/Angelman syndrome 1. | SPG7, paraplegin matrix AAA peptidase subunit. | 0.778 |
PAAF1 | ALDH16A1 | ENSEASP00005026280 | ENSEASP00005006775 | Proteasomal ATPase associated factor 1. | Aldehyde dehydrogenase 16 family member A1. | 0.634 |
PAAF1 | SPG21 | ENSEASP00005026280 | ENSEASP00005009087 | Proteasomal ATPase associated factor 1. | Spastic paraplegia 21 (autosomal recessive, Mast syndrome). | 0.596 |
SPG11 | NIPA1 | ENSEASP00005026397 | ENSEASP00005030692 | Spastic paraplegia 11 (autosomal recessive). | Non imprinted in Prader-Willi/Angelman syndrome 1. | 0.711 |
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