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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
5 zes the transfer of the L-fucose moiety from guanosine diphosphate-beta-L-fucose (GDP-Fuc) to accepto
6 Here, we report a crystal structure of EF4-guanosine diphosphate bound to the Thermus thermophilus
7 factor that converts eIF2, from an inactive guanosine diphosphate-bound complex to eIF2-guanosine tr
9 Guanosine triphosphate-bound Ran, but not guanosine diphosphate-bound Ran, stimulated polymerizati
10 al regulation of Rab7 guanosine triphosphate/guanosine diphosphate cycling occurs by Armus recruitmen
11 mechanism for receptor-catalyzed exchange of guanosine diphosphate for guanosine triphosphate is prop
12 ivation of Ras by catalyzing the exchange of guanosine diphosphate for guanosine triphosphate on Ras.
15 es with the enzyme fucosyltransferase-VI and guanosine diphosphate fucose to enhance the interaction
16 ing pathway between the alpha5 helix and the guanosine diphosphate (GDP) binding pocket remains elusi
17 king in ordered systems, as illustrated with guanosine diphosphate (GDP) bound to ADP ribosylation fa
19 hat was fully dependent on rhodopsin for GTP-guanosine diphosphate (GDP) exchange and showed GTP hydr
21 y NHE1 is not necessary for release of Cdc42-guanosine diphosphate (GDP) from Rho GDP dissociation in
23 locked dominant active Rab4 (Rab4(GTP)), or guanosine diphosphate (GDP) locked dominant inactive Rab
24 -Rab7 exhibited a 3-fold higher affinity for guanosine diphosphate (GDP) relative to guanosine tripho
25 sine triphosphate (ATP)-driven conversion of guanosine diphosphate (GDP), inhibited dynamin-mediated
26 otide-independent curved conformations, both guanosine diphosphate (GDP)-bound and GTP-bound tubulin
27 Ran is a small GTPase that cycles between a guanosine diphosphate (GDP)-bound form (RanGDP) and a gu
28 guanosine triphosphatase (GTPase) Ran in its guanosine diphosphate (GDP)-bound form and to karyopheri
29 eficient and does not cycle between GTP- and guanosine diphosphate (GDP)-bound forms, suggesting that
36 nzymes adenosine diphosphate glucose (ADPG), guanosine diphosphate glucose (GDPG), and cytidine dipho
37 DI from Rab GTPases before Rab activation by guanosine diphosphate-guanosine 5'-triphosphate (GDP-GTP
38 Here, we demonstrate that Rab-activating guanosine diphosphate/guanosine triphosphate exchange fa
41 -O-(3-thio)triphosphate-loaded form, but not guanosine diphosphate-loaded form, binds to the early en
42 duals, we present evidence that mutations in guanosine diphosphate mannose (GDP-mannose) pyrophosphor
43 blasts displayed reductions in PMM activity, guanosine diphosphate mannose, lipid-linked oligosacchar
44 ent systems comprised of glutamate synthase, guanosine diphosphate-mannose pyrophosphorylase, cytidin
46 by controlling the downstream conversion of guanosine diphosphate-Rac to guanosine triphosphate-Rac
48 requires the protein Cyk3, which binds Rho1-guanosine diphosphate via its catalytically inactive tra
49 gomers of indefinite size in the presence of guanosine diphosphate, yields the dependence of the equi
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