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
Histone-lysine N-methyltransferase, H3 lysine-4 specific (1150 aa)
Predicted Functional Partners:
Putative uncharacterized protein (581 aa)
Putative uncharacterized protein (531 aa)
Putative uncharacterized protein (473 aa)
Predicted protein (528 aa)
Putative uncharacterized protein (377 aa)
Transcriptional repressor rco-1 (604 aa)
Predicted protein (200 aa)
Putative uncharacterized protein (677 aa)
Histone-lysine N-methyltransferase, H3 lysine-36 specific (954 aa)
Histone-lysine N-methyltransferase, H3 lysine-79 specific; Histone methyltransferase that specifically methylates histone H3 to form H3K79me. This methylation is required for telomere silencing and for the pachytene checkpoint during the meiotic cell cycle by allowing the recruitment of RAD9 to double strand breaks. Nucleosomes are preferred as substrate compared to free histones (531 aa)
Your Current Organism:
NCBI taxonomy Id: 5141 Other names: Chrysonilia crassa, N. crassa, Neurospora, Neurospora crassa