PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 24091101-2 2014 The SH2 domain containing inositol 5-phosphatases SHIP1 and SHIP2 belong to this family of enzymes that dephosphorylate the 5 position of PI(3,4,5)P3 to produce PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 138-149 inositol polyphosphate-5-phosphatase D Homo sapiens 50-55 23121445-2 2013 BACKGROUND: The SH2-containing inositol-5"-phosphatase 1 (SHIP1) metabolizes PI(3,4,5)P3 to PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 77-88 inositol polyphosphate-5-phosphatase D Homo sapiens 16-56 23551094-2 2013 SHIP1 removes the 5"-phosphate from the product of PI3K, PI(3,4,5)P3, to generate PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 57-68 inositol polyphosphate-5-phosphatase D Homo sapiens 0-5 24069021-4 2013 Consequently, the 5"- and 3"-inositol poly-phosphatases SHIP1, SHIP2, and phosphatase and tensin homolog capable of targeting PI(3,4,5)P3 are potential genetic determinants of T cell effector functions in vivo. phosphoinositide-3,4,5-triphosphate 126-137 inositol polyphosphate-5-phosphatase D Homo sapiens 56-61 24069021-5 2013 In addition, the 5"-inositol poly-phosphatases SHIP1 and 2 can shunt PI(3,4,5)P3 to the rare but potent signaling phosphoinositide species PI(3,4)P2 and thus these SHIP1/2, and the INPP4A/B enzymes that deplete PI(3,4)P2 may have precise roles in T cell biology to amplify or inhibit effectors of PI3K signaling that are selectively recruited to and activated by PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 69-80 inositol polyphosphate-5-phosphatase D Homo sapiens 47-58 24069021-5 2013 In addition, the 5"-inositol poly-phosphatases SHIP1 and 2 can shunt PI(3,4,5)P3 to the rare but potent signaling phosphoinositide species PI(3,4)P2 and thus these SHIP1/2, and the INPP4A/B enzymes that deplete PI(3,4)P2 may have precise roles in T cell biology to amplify or inhibit effectors of PI3K signaling that are selectively recruited to and activated by PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 69-80 inositol polyphosphate-5-phosphatase D Homo sapiens 164-171 23121445-2 2013 BACKGROUND: The SH2-containing inositol-5"-phosphatase 1 (SHIP1) metabolizes PI(3,4,5)P3 to PI(3,4)P2. phosphoinositide-3,4,5-triphosphate 77-88 inositol polyphosphate-5-phosphatase D Homo sapiens 58-63 17442886-8 2007 These results support a model in which phagosomal PI3K generates PI(3,4,5)P(3) necessary for later stages of phagocytosis, PTEN determines whether those late stages can occur, and SHIP-1 regulates when and where they occur by transiently suppressing PI(3,4,5)P(3)-dependent activities necessary for completion of phagocytosis. phosphoinositide-3,4,5-triphosphate 250-263 inositol polyphosphate-5-phosphatase D Homo sapiens 180-186 21056081-2 2011 As a result, SHIP dampens down PI-3,4,5-P(3)-mediated signaling and represses the proliferation, differentiation, survival, activation, and migration of hematopoietic cells. phosphoinositide-3,4,5-triphosphate 31-44 inositol polyphosphate-5-phosphatase D Homo sapiens 13-17 25723258-2 2015 By converting PI(3,4,5)P3 to PtdIns(3,4)P2 at the plasma membrane, SHIP1 modifies PI3-kinase mediated signaling. phosphoinositide-3,4,5-triphosphate 14-25 inositol polyphosphate-5-phosphatase D Homo sapiens 67-72 12529653-7 2003 These results suggest a possible role of the mutated SHIP gene in the development of acute leukemia and chemotherapy resistance through the deregulation of the phosphatidylinositol-3,4,5-triphosphate (PI(3,4,5)P3)/Akt signaling pathway. phosphoinositide-3,4,5-triphosphate 201-212 inositol polyphosphate-5-phosphatase D Homo sapiens 53-57 27760174-8 2016 Thus, our results illustrate the importance of BAR domain proteins in podosome structure and dynamics, and identify a new PSTPIP1/PTPN6/SHIP1/2-dependent negative feedback mechanism that counterbalances Src and PI(3,4,5)P3 signalling to control osteoclast cell polarity and activity during bone resorption. phosphoinositide-3,4,5-triphosphate 211-222 inositol polyphosphate-5-phosphatase D Homo sapiens 136-141