ライフサイエンスコーパス: guanosine 5'-diphosphate

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1 nucleotide (guanosine 5'-triphosphate versus guanosine 5'-diphosphate).

2 GTPgammaS) binding in the presence of excess guanosine 5'-diphosphate.

3 onvergent protein-binding surface of Galphas.guanosine 5'-diphosphate.

4 y at the GTP pocket which is consistent with guanosine 5'-diphosphate 2':3'-cyclic monophosphate.

5 review, we discuss newly elucidated roles of guanosine 5'-diphosphate 3'-diphosphate (ppGpp) in trans

6 Guanosine 5'-diphosphate 3'-diphosphate (ppGpp), a pleio

7 nitiating nucleoside triphosphate (iNTP) and guanosine 5'-diphosphate 3'-diphosphate (ppGpp), the mol

8 howing that changes in the concentrations of guanosine 5'-diphosphate 3'-diphosphate and initiating n

9 proteins (Fis and H-NS) and small molecules (guanosine 5'-diphosphate 3'-diphosphate and initiating n

10 nitiating nucleoside triphosphate (iNTP) and guanosine 5'-diphosphate, 3'-diphosphate (ppGpp) concent

11 ither in wild-type cells or in cells lacking guanosine 5'-diphosphate, 3'-diphosphate, providing insi

12 between reversion rates and the synthesis of guanosine-5'-diphosphate-3'-diphosphate in the absence a

13 nteraction of Ypt1p with guanine nucleotide (guanosine 5'-diphosphate and guanosine 5'-triphosphate/g

14 Once bound, GTP undergoes hydrolysis to form guanosine 5'-diphosphate and inorganic phosphate.

15 onsequently, drugs targeting the inactive or guanosine 5'-diphosphate-bound conformation are not expe

16 re able to interact in similar ways with the guanosine 5'-diphosphate-bound GTPase, but differ in the

17 mpounds (adenosine-5'-diphosphate-D-glucose, guanosine-5'-diphosphate-D-glucose, and thymidine-5'-dip

18 ociation inhibitors RhoGDI and D4GDI inhibit guanosine 5'-diphosphate dissociation from Rho GTPases,

19 differences of the N-terminal domains of the guanosine 5'-diphosphate dissociation inhibitors.

20 guanosine 5'-monophosphate (GMP) and dGMP to guanosine 5'-diphosphate (GDP) and dGDP, respectively.

21 ular docking resulted into identification of guanosine 5'-diphosphate (GDP) as a promising hepcidin-b

22 e protein directly activated by cAMP), a Rap guanosine 5'-diphosphate (GDP) exchange factor.

23 plexes between K-Ras or the G12X mutants and guanosine 5'-diphosphate (GDP) or GDPnP (a stable GTP an

24 orks, but the molecular mechanism underlying guanosine 5'-diphosphate (GDP) release by the G protein

25 , we observed that in solution, farnesylated guanosine 5'-diphosphate (GDP)-bound K-Ras4B is predomin

26 isiae, the Ras-like GTPase Bud1/Rsr1 and its guanosine 5'-diphosphate (GDP)/guanosine 5'-triphosphate

27 -Mn2+-oxaloacetic acid (OAA), -Mn2+-OAA-Mn2+-guanosine-5'-diphosphate (GDP), and -Mn2+-Mn2+-guanosine

28 of vinblastine and guanosine 5'-triphosphate/guanosine 5'-diphosphate, indicating that colchicine sit

29 phate; MANT-GDP, 3',2'-O(N-methylantraniloyl)guanosine-5'-diphosphate; MANT-CDP, 3',2'-O-(N-methylant

30 ases Cdc42, Rac1, RhoA, and Ras and displace guanosine 5'-diphosphate with high intrinsic exchange ra

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