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2 e reaction afforded a single product, and no rotameric and keto-enol isomeric products are formed.
3 center closely around ideal g(-), g(+) and t rotameric angles, even though no rotamer restraint is us
6 f the reconstruction enables identifying the rotameric conformation adopted by some amino-acid side c
8 d geometry, particularly with respect to the rotameric conformation of the ethylamine side chain and
10 chemical shifts for the determination of the rotameric conformation of Val and Leu residues in protei
11 t quality to unambiguously assign amino acid rotameric conformations and identify ordered water molec
12 5R and Arg(72) were stacked in two different rotameric conformations in TFV-DP- and dATP-bound struct
14 s are generally well separated into distinct rotameric conformations, but alternative backbone confor
17 nd beta-D-glucopyranosides reveals different rotameric distributions about their hydroxymethyl groups
18 e 360 kDa 'half-proteasome' where the chi(1) rotameric distributions of Val residues are calculated o
19 when the protein design process incorporates rotameric energy minimization, DEE is no longer provably
22 or the various spin pairs is consistent with rotameric equilibria in the nitroxide side chain, as obs
23 lent interactions to regulate backbone amide rotameric equilibria, including n-->pi*, steric, and hyd
24 ever, only minor differences are seen in the rotameric equilibrium about the C(4)-C(5) bond in 3 and
26 i) aid in distinguishing conformational from rotameric exchange as the origin of the resolved states,
29 ade in establishing that the RNA backbone is rotameric, few libraries of discrete conformations speci
31 lithiation from the lowest energy amide-like rotameric forms (cis for N-thiopivaloyl and trans for N-
32 istinct mechanisms based on Thr-87 or Ile-95 rotameric forms, are observed for the previously identif
33 416) backbone dynamics as well as spin-label rotameric freedom are sensitive to and altered by the pe
34 he hypothesis that residues with constrained rotameric freedom in helical conformation might reduce t
37 f protein tertiary structure, might serve as rotameric molecular switches in other biological process
38 ral and structural studies indicate that the rotameric nature of the Tyr106 residue is involved in ac
43 kcal/mol) likely because of favorable chi(1) rotameric preferences for aromatic residues at C-capping
46 on types such as hinge, shear, twist, screw, rotameric side chains, normal modes and essential dynami
49 e "Y-T coupling" mechanism, wherein the chi1 rotameric state of a highly conserved aromatic residue c
52 also by two state parameters concerning the rotameric state of the residues to which the interacting
53 ve conformation further demonstrate that the rotameric state of Y101 is uncorrelated with the global
57 side chains are assumed to exchange between rotameric states and where the exchange rates and a prio
58 the spin label side chains in terms of their rotameric states are constructed from the trajectories.
59 shifts led to predictions of the side chain rotameric states for several Val and Leu residues in thi
60 and F14, the number of exchanging side-chain rotameric states increases in the HAP-bound complex rela
61 nversion of this tyrosine (Y101) between its rotameric states is actually faster than the rate of ina
63 by direct experimental measurement that the rotameric states of R1 found in this crystal provide a v
65 using a model which proposes that different rotameric states of the indole alanyl side-chain are res
69 ntial which can account for the influence of rotameric states on the specificity of atomic interactio
70 ntial, ROTAS accounting for the influence of rotameric states on the specificity of atomic interactio
71 ion activates transitions between additional rotameric states that are not sampled in the dry protein
74 rofiles, we quantify conformational entropy, rotameric strain energy and chi strain energy for all 17
78 both TM2 and TM5, securing the Trp-356(6.48) rotameric switch and restraining it from activation.
79 ter molecules, and secures the Trp-356(6.48) rotameric switch in the inactive state to promote the fo
80 ivation, this tryptophan residue undergoes a rotameric transition that may be coupled to a series of
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