ライフサイエンスコーパス: G-protein beta subunit

1 t it encodes AGB1, a putative heterotrimeric G-protein beta subunit.

2 s one of the SDD products that encodes a rat G-protein beta subunit.

3 WD repeat structure similar to that of known G protein beta subunits.

4 ype cells overexpressing signaling-defective G protein beta subunits.

5 ranuclearly with DNA encoding five different G-protein beta subunits.

6 To our knowledge, GNB3 encoding the G-protein beta subunit 3 (Gbeta3) has not previously bee

7 GNB5 encodes the G protein beta subunit 5 and is involved in inhibitory G

8 d to the zymogen granule membrane along with G-protein beta-subunit; all three alpha subunits were pr

9 ulatory process that blocks signaling from a G protein beta subunit and causes its relocalization wit

10 ise enhanced upon direct activation of Ste4 (G protein beta subunit) and Ste11 (Ste7 kinase) but not

11 nding in vitro of Ste5 to Ste11, Ste7, Ste4 (G protein beta subunit), and Fus3 (MAPK), confirmed that

12 ificity of interaction of RGS6 and RGS7 with G protein beta subunits, and certain biochemical propert

13 Because all of the G-protein beta subunits are found in the nervous system,

14 f this family include the signal-transducing G protein beta subunit, as well as other proteins that r

15 to hypothesize that Vps15 may function as a G protein beta subunit at the endosome.

16 tes that the posttranslational processing of G protein beta subunits begins inside the protein-foldin

17 which is constitutively bound to the type 5 G protein beta-subunit (beta5).

18 annel indicates that Ca2+ channel beta1b and G protein beta subunits bind to the alpha1 subunit at th

19 ion of the single gene for the Dictyostelium G protein beta-subunit blocks development at an early st

20 These results indicate that individual G protein beta subunit domains can act as independent, s

21 units, or antibodies to different regions of G-protein beta subunits established the involvement of a

22 A structurally divergent G-protein beta subunit expressed in brain and retina, Gb

23 RGS11) interact with the fifth member of the G protein beta-subunit family, Gbeta5.

24 with AC2, the structural determinants on the G protein beta subunit for interaction with various effe

25 The complex of RGS9 with type 5 G protein beta subunit (G beta 5) is abundant in photore

26 with the short splice isoform of the type 5 G-protein beta subunit (G beta 5) and the RGS9 anchor pr

27 The trimeric G-protein beta subunit (G beta) appears to be the most c

28 has the unique ability to interact with the G protein beta subunit Gbeta(5).

29 Here, we report that G protein beta subunits (Gbeta) bind to DDB1 and that Gb

30 s where it forms complexes with the atypical G protein beta subunit, Gbeta(5), and transmembrane prot

31 A G-protein beta subunit, Gbeta(3), plays a critical role

32 ns form trimeric complexes with the atypical G protein beta subunit Gbeta5 and a membrane anchor, R7B

33 The G protein beta subunit Gbeta5 deviates significantly fro

34 The G protein beta subunit Gbeta5 uniquely forms heterodimer

35 l DHEX domain and are obligatory dimers with G protein beta subunit Gbeta5.

36 RGS11, which exist as heterodimers with the G protein beta subunit Gbeta5.

37 ulator of G-protein signaling RGS9-1 and the G-protein beta subunit Gbeta5-L.

38 The type 5 G protein beta subunit (Gbeta5) can form complexes with

39 signaling protein family (RGS9) with type 5 G protein beta subunit (Gbeta5).

40 GS form trimeric complexes with the atypical G protein beta subunit, Gbeta5, and membrane anchor R7BP

41 The G protein beta subunit, Gbeta5, is predominantly express

42 complex with the long splice variant of the G protein beta subunit (Gbeta5L).

43 ling family (RGS9-1) and its partner, type 5 G protein beta-subunit (Gbeta5L).

44 signaling (RGS) protein, RGS9-1, and type 5 G protein beta-subunit, Gbeta5L, regulates the duration

45 The gene encoding a heterotrimeric G-protein beta subunit, GPB1, was cloned and disrupted.

46 accompanied by a parallel redistribution of G protein beta subunits; however, there was no increase

47 In contrast, the G protein beta subunit induces FRET signals on both the

48 rms overexpressing gar-3 or lacking GPB-2, a G-protein beta-subunit involved in RGS-mediated inhibiti

49 olding of the first five beta strands in the G protein beta subunit is a requirement for appropriatel

50 Among the five G protein beta subunits known, the beta(4) subunit type

51 The Lethal with Sec Thirteen 8/G protein beta subunit-like (LST8/GbetaL) protein is a m

52 single gcr1, gpa1, and agb1 (heterotrimeric G-protein beta-subunit) mutants are additive or synergis

53 characterized the modulatory domains of the G protein beta subunit on the recombinant P/Q-type chann

54 nalyzed the binding of Ca2+ channel beta and G protein beta subunits on the two separate binding site

55 We investigated which subtypes of G-protein beta subunits participate in voltage-dependent

56 G-protein beta subunits perform essential neuronal funct

57 structure of another WD repeat protein, the G-protein beta-subunit, predicts that esc protein adopts

58 elopment ensures expression of RGS9-2/type 5 G-protein beta subunit/R7BP complexes at postsynaptic si

59 family and the long splice variant of type 5 G protein beta subunit (RGS9-Gbeta5L) plays a critical r

60 amily with the long splice variant of type 5 G protein beta subunit (RGS9.Gbeta5L).

61 signaling by inhibiting the activity of the G protein beta subunit, Ste4p.

62 d the physiological role of Gbeta5, a unique G protein beta subunit that dimerizes with regulators of

63 in beta-propeller enzymes and is used by the G protein beta subunit to bind the G protein alpha subun

64 Homolog-scanning mutagenesis of the G protein beta subunit was employed to identify residues

65 at phenotypically resemble cells lacking the G-protein beta-subunit yielded the protein kinase YakA.