BAIT
INPP5D
SHIP, SHIP-1, SHIP1, SIP-145, p150Ship, s-SHIP
inositol polyphosphate-5-phosphatase D
GO Process (19)
GO Function (6)
GO Component (5)
Gene Ontology Biological Process
- dephosphorylation [IDA]
- determination of adult lifespan [IMP]
- immunoglobulin mediated immune response [IMP]
- intracellular signal transduction [IMP]
- negative regulation of B cell activation [IMP]
- negative regulation of B cell proliferation [IMP]
- negative regulation of bone resorption [IMP]
- negative regulation of cell proliferation [IDA]
- negative regulation of granulocyte differentiation [IMP]
- negative regulation of immune response [IMP]
- negative regulation of interleukin-6 biosynthetic process [IMP]
- negative regulation of monocyte differentiation [IMP]
- negative regulation of neutrophil differentiation [IMP]
- negative regulation of osteoclast differentiation [IMP]
- negative regulation of signal transduction [IMP]
- positive regulation of B cell differentiation [IMP]
- positive regulation of apoptotic process [IMP]
- positive regulation of erythrocyte differentiation [IMP]
- positive regulation of lymphocyte differentiation [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Mus musculus
PREY
SEC23A
Msec23, Sec23r
SEC23A (S. cerevisiae)
GO Process (1)
GO Function (1)
GO Component (5)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Mus musculus
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Src homology 2 (SH2)-containing 5'-inositol phosphatase localizes to podosomes, and the SH2 domain is implicated in the attenuation of bone resorption in osteoclasts.
c-Src plays an important role in bone resorption by osteoclasts. Here, we show using wild-type and ship(-/-) osteoclasts that Src homology 2 (SH2)-containing 5'-inositol phosphatase (SHIP) appeared to negatively regulate bone resorption activated by c-Src. SHIP was found to localize to podosomes under the influence of c-Src, and the presence of either the amino-terminal region comprising the SH2 domain or ... [more]
Endocrinology Jul. 01, 2006; 147(7);3307-17 [Pubmed: 16601135]
Throughput
- Low Throughput
Curated By
- BioGRID