Find Molecular Interactions in the Scientific Literature
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Result Statistics
Result statistics
Number unique A-genes1
Number unique B-genes1
Number unique A-B gene pairs0
Total number of interactions7
Top Interactions
A-argumentB-argumentcount
YWHAQnone7
A-list mapping 1 0
inputrecognized symbolmapping type
10971YWHAQOrthology Cluster
Interaction Partner Distribution A-List (Pie)
Interaction Partner Distribution A-List (Bars)
Most Frequent Interactions
Interactions with Common Partners
Table View
Gene A SymbolGene B SymbolGene A Gene IDGene B Gene IDRelation TypesFactualityFulltext Match SourceDocument IDContext
YWHAQ 10971 Phosphorylation
   
none9794375
 Furthermore, activation-dependent tyrosine phosphorylation of HS1 was not required for NFAT transcriptional activation.
YWHAQ 10971 Phosphorylation, Regulation
   
none9794375
 Costimulation through CD28 and/or CD2 did not modulate the CD3-dependent phosphorylation of HS1.
YWHAQ 10971 Phosphorylation, Positive_regulation
   
none9794375
 Ligation of CD3 also induces the tyrosine phosphorylation of HS1, a 75-kDa hematopoietic cell-specific intracellular signaling protein of unknown function.
YWHAQ 10971 Phosphorylation
   
none9794375
 Uncoupling activation-dependent HS1 phosphorylation from nuclear factor of activated T cells transcriptional activation in Jurkat T cells: differential signaling through CD3 and the costimulatory receptors CD2 and CD28.
YWHAQ 10971 Phosphorylation, Positive_regulation
   
none9794375
 Unlike ligation of CD3, stimulation with anti-CD28 mAb or CHO cells expressing the CD28 ligands CD80 or CD86 did not lead to tyrosine phosphorylation of HS1 in Jurkat T cells.
YWHAQ 10971 Phosphorylation, Regulation
   
none9794375
 We have examined changes in HS1 phosphorylation after differential stimulation of CD3, CD2, and CD28 to elucidate its role in T cells and to further delineate the signaling pathways recruited by these receptors.
YWHAQ 10971 Phosphorylation, Positive_regulation
   
none9794375
 Additionally, no tyrosine phosphorylation of HS1 was induced by mitogenic pairs of anti-CD2 mAbs capable of activating the transcription factor NFAT (nuclear factor of activated T cells).