Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Combined Automated Annotation using Multiple IEA Methods
An essential role for BLNK in human B cell development.
Tyrosine residues in phospholipase Cgamma 2 essential for the enzyme function in B-cell signaling.
Human SLP-65 isoforms contribute differently to activation and apoptosis of B lymphocytes.
Solution structure and phosphopeptide binding of the SH2 domain from the human Bruton's tyrosine kinase.
The B-cell antigen receptor signals through a preformed transducer module of SLP65 and CIN85.
SCIMP, a transmembrane adaptor protein involved in major histocompatibility complex class II signaling.
Enhanced prediction of Src homology 2 (SH2) domain binding potentials using a fluorescence polarization-derived c-Met, c-Kit, ErbB, and androgen receptor interactome.
Macromolecular assembly of the adaptor SLP-65 at intracellular vesicles in resting B cells.
Tripartite phase separation of two signal effectors with vesicles priming B cell responsiveness.
Identification of two tyrosine phosphoproteins, pp70 and pp68, which interact with phospholipase Cgamma, Grb2, and Vav after B cell antigen receptor activation.
BLNK: a central linker protein in B cell activation.
BLNK (SLP-65) Signalosome hydrolyzes phosphatidyinositol bisphosphate forming diacylglycerol and inositol-1,4,5-trisphosphate
Phosphorylated BLNK (SLP65, in Antigen:p-BCR:p-SYK:p-BLNK:CIN85:GRB2:SOS1) binds BTK, PLCG2, VAV1, NCK1
p-6Y-SYK phosphorylates BLNK (SLP65)
A novel mechanism for the autonomous termination of pre-B cell receptor expression via induction of lysosome-associated protein transmembrane 5.