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1 e ATP analogue ADPNP (5'-adenylyl beta,gamma-imidodiphosphate).
2 (addition of MgCl2 + 5'-adenylyl-beta,gamma-imidodiphosphate).
3 2) determined with or without bound adenylyl imidodiphosphate.
4 trate analogs beryllium fluoride or adenylyl-imidodiphosphate.
5 oils with a nonhydrolyzable analog, adenylyl imidodiphosphate.
6 yzable analog of ATP, 5'-adenylyl-beta,gamma-imidodiphosphate.
7 PPases in a ternary complex with Mg(2+) and imidodiphosphate.
8 denosine 5'-O-(3-thiotriphosphate) or adenyl-imidodiphosphate.
9 5'-triphosphate (GTP) analogue, 5'-guanylyl-imidodiphosphate.
10 vitro by ATP and the ATP analog adenyl-5'-yl imidodiphosphate.
11 ed in the presence of 5'-adenylyl beta,gamma-imidodiphosphate.
12 the nonhydrolyzable ATP analogue 5'-adenylyl imidodiphosphate.
13 ce of nonhydrolyzable 5'-adenylyl-beta,gamma-imidodiphosphate, a third state, which is identical with
14 eotide analogs, ADP, 5'-adenylyl-beta, gamma-imidodiphosphate, adenosine 5'-(beta,gammaimino)triphosp
15 lyzable ATP analogue 5'-adenylyl-beta, gamma-imidodiphosphate (ADPNP) to Escherichia coli DNA gyrase
19 ration of the ATP binding site with adenylyl imidodiphosphate afforded protection against photolabeli
20 ex in the presence of 5'-adenylyl-beta,gamma-imidodiphosphate, albeit with a lower efficiency than th
21 able analogs of ATP, 5'-adenylyl beta, gamma-imidodiphosphate (AMP-PNP) and adenosine 5'-(alpha, beta
23 P and the non-hydrolysable analogue adenylyl imidodiphosphate (AMP-PNP) partially substituted for ATP
25 drolyzable ATP analog 5'-adenylyl-beta,gamma-imidodiphosphate (AMP-PNP) similarly stabilize the packa
26 logues of ATP, ADP, and 5'-adenyl-beta,gamma-imidodiphosphate (AMP-PNP) with the two domains of funct
27 TP is two times more effective than adenylyl imidodiphosphate (AMP-PNP), a hydrolysis-resistant ATP a
28 ) as did replacing pipette ATP with adenylyl imidodiphosphate (AMP-PNP), a non-hydrolysable analogue.
29 Delay of closing in wild type by adenylyl imidodiphosphate (AMP-PNP), a non-hydrolysable ATP analo
31 nhydrolyzable analog 5'-adenylyl-beta, gamma-imidodiphosphate (AMP-PNP), ADP, or ADP + Pi using both
32 mogenates with ATP or its analogue, adenylyl imidodiphosphate (AMP-PNP), is required for the strong a
33 ADPs was replaced with adenylyl beta, gamma-imidodiphosphate (AMP-PNP), some protection from cold di
34 ATP analog, adenosine 5'-adenylyl-beta,gamma-imidodiphosphate (AMP-PNP), was determined at 2.6 A reso
35 lyzable ATP analogue, 5'-adenylyl beta,gamma-imidodiphosphate (AMP-PNP), was investigated by using th
36 cellular ATP, as well as GTP and 5'-adenylyl-imidodiphosphate (AMP-PNP), were accompanied by a corres
37 lyzable ATP analogue, 5'-adenylyl-beta,gamma-imidodiphosphate (AMP-PNP), which in the gating models w
38 us-end vesicle motor followed by 5'-adenylyl imidodiphosphate (AMP-PNP)-induced microtubule affinity
41 erivatives of ADP and 5'-adenylyl-beta,gamma-imidodiphosphate (AMPPNP) also indicate an interaction s
44 hate (AMP), and of an ATP analogue, adenylyl imidodiphosphate (AMPPNP), bound to Escherichia coliaden
47 y relevant complexes, 5'-adenylyl-beta,gamma-imidodiphosphate (AMPPNP).Mg(2+), AMPPNP.Mg(2+).pantothe
48 f the nonhydrolyzable ATP analogues adenylyl-imidodiphosphate and adenosine 5'-O-thiotriphosphate.
49 nhibited by KF, by the pyrophosphate analogs imidodiphosphate and aminomethylenediphosphonate (AMDP),
50 hate analogs aminomethylenediphosphonate and imidodiphosphate and by KF and N-ethylmaleimide in a dos
51 M of the kinesin inhibitor AMP-PNP (adenylyl-imidodiphosphate) and by anti-kinesin antibody but only
52 strong binding of S-1.MgAMP-PNP (5'-adenylyl imidodiphosphate) and on the weak binding of S-1.MgADP.P
54 by isoproterenol, sodium fluoride, guanyl-5'-imidodiphosphate, and forskolin in hypoxic membranes was
56 onfirmed by the presence of four 5'-adenylyl-imidodiphosphate-binding sites (K(D) = 4.1 x 10(-6)m) pe
57 well to the binding affinity to the guanylyl imidodiphosphate-bound Cdc42, suggesting a rapid equilib
58 well to the binding affinity to the guanylyl imidodiphosphate-bound Rac1, which ranges from 10.5 to 4
59 insensitive to ATP or 5'-adenylyl-beta,gamma-imidodiphosphate but was blocked by ADP-AlF3 or ADP-vana
60 C]Phe-tRNA-elongation factor Tu.guanyl-5'-yl imidodiphosphate) but not [14C]Phe-tRNA.elongation facto
61 d by the nonhydrolyzable GTP analog guanylyl imidodiphosphate by a Ran mutant that is unable to hydro
62 ate analogs, amynomethylenediphosphonate and imidodiphosphate, by dicyclohexylcarbodiimide, and by th
64 nase and its AMP-PNP (5'-adenylyl-beta,gamma-imidodiphosphate) complex to 2.1-angstroms resolutions.
65 e locked in an ADP or 5'-adenylyl-beta,gamma-imidodiphosphate conformation by the cross-linking with
66 lysis of the intact SGS revealed an adenylyl imidodiphosphate-dependent change in protection in the r
67 -(3-thiotriphosphate) (ATPgammaS) and adenyl-imidodiphosphate, each stabilized the primer recognition
68 drolyzable ATP analog 5'-adenylyl-beta,gamma-imidodiphosphate exhibits altered DNA gate dynamics, but
69 ls was found to be activated by guanyl-5'-yl imidodiphosphate (GMPPNP) and was identified as an effec
70 Gialpha1 were: mGTPgammaS > MANT-5'-guanylyl-imidodiphosphate > MANT-guanylyl-(beta,gamma-methylene)-
71 n II ATP-Mg(2+) = ATP = AMP-PNP (5'-adenylyl imidodiphosphate) > pyrophosphate = tripolyphosphate > t
72 A new class of highly acidic confined imino-imidodiphosphate (iIDP) Bronsted acids catalyze the asym
73 d even in the presence of Ca(2+) or adenylyl-imidodiphosphate, indicating that the mechanism of stimu
75 hydrolysable analogue 5'-adenylyl beta,gamma-imidodiphosphate, microcin B17 stabilises a gyrase-depen
78 imido analogue of the product pyrophosphate, imidodiphosphate (O(3)P-NH-PO(3)(4)(-)) also displays sl
79 g(2+) coordinated to 5'-adenylyl beta, gamma-imidodiphosphate or ADP bound to catalytic sites of beta
81 x with the ATP analog 5'-adenylyl beta,gamma-imidodiphosphate or the nucleoside sangivamycin crystall
83 '-adenylyl methylenediphosphate, 5'-adenylyl imidodiphosphate, or 5'-adenylyl-O-(3-thiotriphos-phate)
84 ging CFTR activity with vanadate or adenylyl-imidodiphosphate, or by introducing the Walker A mutatio
87 e presence of AMPPNP (5'-adenylyl-beta,gamma-imidodiphosphate), providing a direct linkage between st
89 he presence of pyrophosphate, phosphate, and imidodiphosphate, the numbers of interaction curves were
90 -substrate ATP analog 5'-adenylyl-beta,gamma-imidodiphosphate verified that ATP hydrolysis was requir
91 the ATP phosphorylation antagonist adenylyl-imidodiphosphate, with an ED50 of approximately 0.1 nM.
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