Known metabolic pathways, protein complexes, signal transduction pathways, etc ... from curated databases.
Genes that are sometimes fused into single open reading frames.
STRING allows inspection of the interaction evidence for any given network. Choose any of the viewers above (disabled if not applicable in your network).
Network nodes represent proteins
splice isoforms or post-translational modifications are collapsed, i.e. each node represents all the proteins produced by a single, protein-coding gene locus.
colored nodes: query proteins and first shell of interactors
white nodes: second shell of interactors
empty nodes: proteins of unknown 3D structure
filled nodes: some 3D structure is known or predicted
Edges represent protein-protein associations
associations are meant to be specific and meaningful, i.e. proteins jointly contribute to a shared function; this does not necessarily mean they are physically binding each other.
from curated databases
annotation not available (335 aa)
Predicted Functional Partners:
DNA mismatch repair protein MutS; This protein is involved in the repair of mismatches in DNA. It is possible that it carries out the mismatch recognition step. This protein has a weak ATPase activity (855 aa)
16,7 kDa protein in recA 5’region; cinA_cterm- competence/damage-inducible CinA C-terminal domain protein; Belongs to the CinA family (168 aa)
annotation not available (350 aa)
annotation not available (461 aa)
Rhamnosyltran- rhamnosyltransferase family protein (325 aa)
Ferredoxin; FAD linked oxidase, C-terminal domain protein (938 aa)
Uncharacterized protein (1088 aa)
Pal_lipo- peptidoglycan-associated lipoprotein; Belongs to the ompA family (168 aa)