DOK2
DOK2 (Docking protein 2) هوَ بروتين يُشَفر بواسطة جين DOK2 في الإنسان.[1][2][3]
المراجع
- "Molecular cloning and characterization of p56dok-2 defines a new family of RasGAP-binding proteins"، J Biol Chem، 273 (9): 4827–30، مارس 1998، doi:10.1074/jbc.273.9.4827، PMID 9478921.
- "Differential proteome analysis of TRAP-activated platelets: involvement of DOK-2 and phosphorylation of RGS proteins"، Blood، 103 (6): 2088–95، مارس 2004، doi:10.1182/blood-2003-07-2392، PMID 14645010.
- "Entrez Gene: DOK2 docking protein 2, 56kDa"، مؤرشف من الأصل في 05 ديسمبر 2010.
قراءة متعمقة
- "IL-4/IL-13 signaling beyond JAK/STAT."، J. Allergy Clin. Immunol.، 105 (6 Pt 1): 1063–70، 2000، doi:10.1067/mai.2000.107604، PMID 10856136.
- "The Tek/Tie2 receptor signals through a novel Dok-related docking protein, Dok-R."، Oncogene، 17 (9): 1097–108، 1998، doi:10.1038/sj.onc.1202115، PMID 9764820.
- "Recruitment of Dok-R to the EGF receptor through its PTB domain is required for attenuation of Erk MAP kinase activation."، Curr. Biol.، 9 (18): 1057–60، 2000، doi:10.1016/S0960-9822(99)80458-8، PMID 10508618.
- "Evidence that Llck-mediated phosphorylation of p56dok and p62dok may play a role in CD2 signaling."، J. Biol. Chem.، 275 (19): 14590–7، 2000، doi:10.1074/jbc.275.19.14590، PMID 10799545.
- "The phosphatidylinositol polyphosphate 5-phosphatase SHIP1 associates with the dok1 phosphoprotein in bcr-Abl transformed cells."، Cell. Signal.، 12 (5): 317–26، 2000، doi:10.1016/S0898-6568(00)00073-5، PMID 10822173.
- "p62dok negatively regulates CD2 signaling in Jurkat cells."، J. Immunol.، 166 (7): 4408–15، 2001، doi:10.4049/jimmunol.166.7.4408، PMID 11254695.
- "Novel p62dok family members, dok-4 and dok-5, are substrates of the c-Ret receptor tyrosine kinase and mediate neuronal differentiation."، J. Cell Biol.، 154 (2): 345–54، 2001، doi:10.1083/jcb.200102032، PMC 2150770، PMID 11470823.
- "Dok-R plays a pivotal role in angiopoietin-1-dependent cell migration through recruitment and activation of Pak."، EMBO J.، 20 (21): 5919–28، 2001، doi:10.1093/emboj/20.21.5919، PMC 125712، PMID 11689432.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences."، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Profiling of tyrosine phosphorylation pathways in human cells using mass spectrometry."، Proc. Natl. Acad. Sci. U.S.A.، 100 (2): 443–8، 2003، doi:10.1073/pnas.2436191100، PMC 141014، PMID 12522270.
- "A unique autophosphorylation site on Tie2/Tek mediates Dok-R phosphotyrosine binding domain binding and function."، Mol. Cell. Biol.، 23 (8): 2658–68، 2003، doi:10.1128/MCB.23.8.2658-2668.2003، PMC 152553، PMID 12665569.
- "Dok-R binds c-Abl and regulates Abl kinase activity and mediates cytoskeletal reorganization."، J. Biol. Chem.، 278 (32): 30170–9، 2003، doi:10.1074/jbc.M301339200، PMID 12777393.
- "Functional interaction of RasGAP-binding proteins Dok-1 and Dok-2 with the Tec protein tyrosine kinase."، Oncogene، 23 (8): 1594–8، 2004، doi:10.1038/sj.onc.1207283، PMID 14647425.
- "Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry."، Anal. Chem.، 76 (10): 2763–72، 2004، doi:10.1021/ac035352d، PMID 15144186.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells."، Nat. Biotechnol.، 23 (1): 94–101، 2005، doi:10.1038/nbt1046، PMID 15592455.
- "Dok-R mediates attenuation of epidermal growth factor-dependent mitogen-activated protein kinase and Akt activation through processive recruitment of c-Src and Csk."، Mol. Cell. Biol.، 25 (9): 3831–41، 2005، doi:10.1128/MCB.25.9.3831-3841.2005، PMC 1084282، PMID 15831486.
بوابة طب
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
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