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1 whereas the other is soluble but fused to a G-protein gamma-subunit.
2 ant of the interaction between receptors and G protein gamma subunits.
3 nding partners that function in the place of G protein gamma subunits.
4 roteins including Rho, Rap1, Rac, Cdc42, and G-protein gamma subunits.
5 ously reported a role for the heterotrimeric G protein gamma subunit 1 (Ggamma1) in mediating cardial
6 confirmation of a role of the heterotrimeric G-protein gamma subunit, AGG3, in cold tolerance, as new
7 shown to contain an endogenous translocating G protein gamma subunit and exhibit receptor-induced Gol
8 ect cells properly process the CaaX motif in G protein gamma subunits and are a useful model system t
9 ribe a new C-terminal processing pattern for G protein gamma subunits and establish the principle tha
10 mily of small GTPases and the heterotrimeric G protein gamma subunit are methylated on their carboxy-
12 coded for in the human genome, including all G protein gamma subunits, are predicted to be prenylated
13 here that a peptide from the C terminus of a G protein gamma subunit blocks muscarinic receptor-stimu
14 tially destroyed, interacted poorly with the G protein gamma subunit but effectively with domains of
15 ma subunits and establish the principle that G protein gamma subunits can be heterogeneously modified
16 tem to directly test the hypothesis that the G protein gamma subunits contribute to the specificity o
17 key component of ASH adaptation is GPC-1, a G-protein gamma-subunit expressed specifically in chemos
18 eptides specific to two other members of the G protein gamma subunit family are significantly less ef
19 ation showed that 6 of the 12 members of the G protein gamma subunit family translocate specifically
20 elucidates a mechanism for the targeting of G protein gamma subunits for ubiquitylation and degradat
21 e we demonstrate that the two heterotrimeric G-protein gamma-subunits from Arabidopsis (Arabidopsis t
22 identified in bovine retinas a cone-specific G-protein gamma subunit (G gamma c, previously named G g
23 ossible exception of gamma1 and gamma11, the G protein gamma subunit genes are well dispersed within
27 -translational prenylation of heterotrimeric G protein gamma subunits is essential for high affinity
28 everal RGS proteins, including RGS9, contain G protein gamma-subunit like domain that can mediate the
29 o)alpha, DGK-1 diacylglycerol kinase, EAT-16 G protein gamma subunit-like (GGL)-containing RGS protei
31 EP (disheveled, EGL-10, pleckstrin) and GGL (G protein gamma subunit-like) domains form a subfamily t
32 EP (disheveled, Egl-10, pleckstrin) and GGL (G protein gamma subunit-like) domains in addition to the
33 EP (disheveled, Egl-10, pleckstrin) and GGL (G protein gamma subunit-like) domains in addition to the
34 heveled/Egl-10/pleckstrin) homology and GGL (G protein gamma-subunit-like) domains in addition to the
35 nhanced in the presence of a mutation in the G protein (gamma) subunit of eIF2, gcd11-K250R, which mi
37 proteins such as Ras, most Rho GTPases, and G protein gamma subunits, plays an essential role in det
38 re supports a direct interaction between the G protein gamma subunit prenyl group and PLCbeta isozyme
40 These results support a specific role for G protein gamma subunit types in signal transduction, mo
41 ion of the posttranslational modification of G-protein gamma subunits via nonreceptor-mediated activa