ライフサイエンスコーパス: guanosine diphosphate

1 Comparable results were seen with [(14)C]guanosine diphosphate.

2 e Ras-guanosine triphosphate to inactive Ras-guanosine diphosphate.

3 onvert adenosylcobinamide (AdoCbi) to AdoCbi-guanosine diphosphate (AdoCbi-GDP) via an AdoCbi-phospha

4 transferase activity, it specifically binds guanosine diphosphate and adenosine diphosphate.

5 dimeric conformations upon binding to GTP or guanosine diphosphate, and that the Parkinson's disease

6 zes the transfer of the L-fucose moiety from guanosine diphosphate-beta-L-fucose (GDP-Fuc) to accepto

7 Here, we report a crystal structure of EF4-guanosine diphosphate bound to the Thermus thermophilus

8 factor that converts eIF2, from an inactive guanosine diphosphate-bound complex to eIF2-guanosine tr

9 ve guanosine triphosphate-bound and inactive guanosine diphosphate-bound forms.

10 s a ligand-binding pocket and has captured a guanosine diphosphate-bound inactive Gi through a tenuou

11 Conversely, expression of a guanosine diphosphate-bound Rag mutant prevented stimula

12 Guanosine triphosphate-bound Ran, but not guanosine diphosphate-bound Ran, stimulated polymerizati

13 By contrast, in the posthydrolysis, guanosine diphosphate-bound state, these helices are rep

14 al regulation of Rab7 guanosine triphosphate/guanosine diphosphate cycling occurs by Armus recruitmen

15 otein to open into its active form, with the guanosine diphosphate exposed for signaling.

16 mechanism for receptor-catalyzed exchange of guanosine diphosphate for guanosine triphosphate is prop

17 ivation of Ras by catalyzing the exchange of guanosine diphosphate for guanosine triphosphate on Ras.

18 G protein alpha (Galpha) subunit to exchange guanosine diphosphate for guanosine triphosphate.

19 diate between the guanosine triphosphate and guanosine diphosphate forms.

20 es with the enzyme fucosyltransferase-VI and guanosine diphosphate fucose to enhance the interaction

21 Family 35 Member C1 (SLC35C1) can transport Guanosine diphosphate-fucose into the Golgi to facilitat

22 ing pathway between the alpha5 helix and the guanosine diphosphate (GDP) binding pocket remains elusi

23 king in ordered systems, as illustrated with guanosine diphosphate (GDP) bound to ADP ribosylation fa

24 Guanosine diphosphate (GDP) dissociation inhibitors (GDI

25 hat was fully dependent on rhodopsin for GTP-guanosine diphosphate (GDP) exchange and showed GTP hydr

26 Bud3 catalyzes the release of guanosine diphosphate (GDP) from Cdc42 and elevates intr

27 y NHE1 is not necessary for release of Cdc42-guanosine diphosphate (GDP) from Rho GDP dissociation in

28 Treatment of CB CD34(+) cells with guanosine diphosphate (GDP) fucose and exogenous alpha1-

29 nversion of guanosine triphosphate (GTP) and guanosine diphosphate (GDP) is known to be integral to a

30 locked dominant active Rab4 (Rab4(GTP)), or guanosine diphosphate (GDP) locked dominant inactive Rab

31 -Rab7 exhibited a 3-fold higher affinity for guanosine diphosphate (GDP) relative to guanosine tripho

32 ctive, agonist and G(s)-bound state, and the guanosine diphosphate (GDP) release from G(s).

33 sine triphosphate (ATP)-driven conversion of guanosine diphosphate (GDP), inhibited dynamin-mediated

34 otide-independent curved conformations, both guanosine diphosphate (GDP)-bound and GTP-bound tubulin

35 Ran is a small GTPase that cycles between a guanosine diphosphate (GDP)-bound form (RanGDP) and a gu

36 guanosine triphosphatase (GTPase) Ran in its guanosine diphosphate (GDP)-bound form and to karyopheri

37 (S-IIP) that is present only in the inactive guanosine diphosphate (GDP)-bound form of KRAS(G12C), sp

38 eficient and does not cycle between GTP- and guanosine diphosphate (GDP)-bound forms, suggesting that

39 T2/6/7 has a modest preference for GTP- over guanosine diphosphate (GDP)-bound MT lattice and compete

40 GPSM2 keeps GNAI in a guanosine diphosphate (GDP)-bound state, but how GPSM2-G

41 AS(G12C) inhibitors bind to the inactive, or guanosine diphosphate (GDP)-bound, state of the oncoprot

42 to necks of budding endocytic vesicles, in a guanosine diphosphate (GDP)-bound, super-constricted sta

43 Guanosine diphosphate (GDP)-dissociation inhibitors (GDI

44 BACKGROUND & AIMS: De novo synthesis of guanosine diphosphate (GDP)-fucose, a substrate for fuco

45 De novo synthesis of guanosine diphosphate (GDP)-fucose, a substrate for fuco

46 Vav, a guanosine diphosphate (GDP)-guanosine triphosphate (GTP)

47 growth cone MTs and is excluded from the GTP/guanosine diphosphate (GDP)-inorganic phosphate (Pi) cap

48 Plants synthesize ascorbate from guanosine diphosphate (GDP)-mannose via L-galactose/L-gu

49 of guanosine triphosphate (GTP)-MTs than on guanosine diphosphate (GDP)-MTs.

50 es and identify guanylate kinase 1 (GUK1), a guanosine diphosphate (GDP)-synthesizing enzyme, as a ta

51 EF2a at its N-terminal S86, which stimulates guanosine diphosphate (GDP)-to-GTP exchange to activate

52 went hydrolysis to produce microtubule-bound guanosine diphosphate (GDP).

53 nzymes adenosine diphosphate glucose (ADPG), guanosine diphosphate glucose (GDPG), and cytidine dipho

54 DI from Rab GTPases before Rab activation by guanosine diphosphate-guanosine 5'-triphosphate (GDP-GTP

55 Here, we demonstrate that Rab-activating guanosine diphosphate/guanosine triphosphate exchange fa

56 Several Sec proteins including a guanosine diphosphate/guanosine triphosphate exchange fa

57 activating Ras into inactive Ras is bound to guanosine diphosphate, inactivating Ras.

58 ion of KRas-G12C cells treated with Ras-G12C-guanosine-diphosphate inhibitors underwent adaptive sign

59 -O-(3-thio)triphosphate-loaded form, but not guanosine diphosphate-loaded form, binds to the early en

60 duals, we present evidence that mutations in guanosine diphosphate mannose (GDP-mannose) pyrophosphor

61 blasts displayed reductions in PMM activity, guanosine diphosphate mannose, lipid-linked oligosacchar

62 ent systems comprised of glutamate synthase, guanosine diphosphate-mannose pyrophosphorylase, cytidin

63 ab1b that is commonly dictated by binding to guanosine diphosphate or guanosine triphosphate.

64 Dominant-negative expression of guanosine diphosphate-Rab6 suppressed ZW10 knockdown ind

65 by controlling the downstream conversion of guanosine diphosphate-Rac to guanosine triphosphate-Rac

66 de exchange factor recruited to beads by Ran-guanosine diphosphate (Ran-GDP).

67 Guanosine triphosphate (GTP) turnover, guanosine diphosphate release, GTP binding, and G protei

68 Gq/11/14 subfamily by interfering with GDP (guanosine diphosphate) release, but by an unknown biophy

69 requires the protein Cyk3, which binds Rho1-guanosine diphosphate via its catalytically inactive tra

70 gomers of indefinite size in the presence of guanosine diphosphate, yields the dependence of the equi