ライフサイエンスコーパス: G-alpha-s

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1 G alpha s did not colocalize with TGN38 or caveolin, sug

2 G alpha s was largely restricted to TGN-enriched fractio

3 hion via prostaglandin receptors to activate G alpha s and increase cAMP.

4 of the human prostacyclin receptor (IP) and G alpha s protein have been identified.

5 a prompted intriguing speculations on the IP/G alpha s coupling which mediates vasodilatation and inh

6 cted against G alpha q and G alpha o but not G alpha s and G alpha i precipitated specific alpha 1-AR

7 This assay provides a measurement of G alpha s-adenylyl cyclase interaction that does not rel

8 crease in the level of the 45 kDa subtype of G alpha s and in prefrontal cortex (8/9) there was a sig

9 protein sequence) of the G alpha s protein (G alpha s-Ct), were determined by 2D 1H NMR spectroscopy

10 t with members of other G alpha subfamilies, G alpha s, G alpha q, and G alpha 12/13.

11 These data indicate that G alpha s, G alpha q/11, and G alpha i3 associate with G

12 increasing cAMP production, indicating that G alpha s is activated by these nucleotides.

13 We show that G alpha s, G alpha i3 and G alpha q/11 are present in Go

14 lize with TGN38 or caveolin, suggesting that G alpha s is associated with a distinct population of me

15 me that removes palmitate from H-Ras and the G alpha s subunits of heterotrimeric GTP-binding protein

16 The N-terminal domain (Q384-Q390 in the G alpha s protein) of the peptide adopted an alpha-helic

17 e of the C-terminal domain (Q390-E392 in the G alpha s protein) of the peptide was destabilized upon

18 s (Q384-L394 in the protein sequence) of the G alpha s protein (G alpha s-Ct), were determined by 2D

19 P1 domain and the C-terminal residues of the G alpha s protein in the receptor/G protein coupling.

20 hand, the solution structural models of the G alpha s-Ct peptide in the absence and presence of the

21 Arg45 was observed upon the addition of the G alpha s-Ct peptide.

22 We now report that ligation of the G alpha s-linked adenosine receptors on the cells of an

23 elationship of the iLP1 in coupling with the G alpha s protein, the solution structures of a constrai

24 s in striatal or frontal cortex membranes to G alpha s is markedly reduced, although coupling of [3H]

25 ed on PM but not on Golgi membranes, whereas G alpha s and G alpha i3 were readily detected on both G

26 Antisera against a common sequence within G alpha s, G alpha i, and G alpha o showed no immunoreac

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