ライフサイエンスコーパス: hydrogen bonding

1 hich confirm a persistent key intramolecular hydrogen bonding.

2 ulations to directly observe the presence of hydrogen bonding.

3 groups in the amine that can participate in hydrogen bonding.

4 of the strengths of electronic coupling and hydrogen bonding.

5 it was almost irreversible, probably due to hydrogen bonding.

6 (S/T) residues that have a high capacity for hydrogen bonding.

7 s has usually been associated with OH and NH hydrogen bonding.

8 re restrained by base stacking and base-pair hydrogen bonding.

9 compounds also exhibited binding by multiple hydrogen bonding.

10 e form of a cryptand-like cage using only CH hydrogen bonding.

11 ,2'-bipyrene unit when they interact through hydrogen bonding.

12 uble-helical intermolecular and transannular hydrogen bonding.

13 ond rotation (RIR) via intra- and interlayer hydrogen bonding.

14 uted to intermediates stabilized by enhanced hydrogen bonding.

15 ng to the strong pai-overlap enforced by the hydrogen-bonding.

16 Depending on the reaction pair, hydrogen bonding (1), NH-insertion (2,3), or proton tran

17 mogeneous, highly interconnected in-plane 2D hydrogen bonding (2D-HB) network at the ionic interface,

18 imple and rapid tool to quantify and predict hydrogen-bonding abilities for the design and applicatio

19 tructure and secondary effects contribute to hydrogen-bonding ability and catalysis.

20 1)P NMR binding experiments predicted strong hydrogen-bonding ability, for which catalytic activity w

21 The hydrogen-bonding activation for 66 organocatalysts has b

22 halogen interaction through its sigma-hole, hydrogen bonding also has a significant impact.

23 on of three investigated PBIs, which contain hydrogen-bonding amide side groups in imide position and

24 f the nucleus growing through intermolecular hydrogen bonding among molecular components.

25 Further hydrogen-bonding analyses suggest the formation of hydro

26 ing in part to their similar capacity toward hydrogen bonding and ability to reliably engender define

27 auxiliaries that form robust intermolecular hydrogen bonding and are tethered to naphthalic anhydrid

28 r interaction energy for halogen rather than hydrogen bonding and by an electron density topology ana

29 Chemical retention mechanisms, including hydrogen bonding and calcium bridging, are proposed and

30 Designed hydrogen bonding and dendritic architecture break the pa

31 he structural details, including the role of hydrogen bonding and dimensionality, as well as the opti

32 The formation of dimers due to hydrogen bonding and dispersion forces was observed as w

33 ugh an Ala substitution locally destabilized hydrogen bonding and enhanced mobility, it did not signi

34 low controlled programming of supramolecular hydrogen bonding and facile tuning of crystallization of

35 rystal via the synergistic interplay between hydrogen bonding and hydrophobic groups, in stark contra

36 the assembly of Abeta oligomers is driven by hydrogen bonding and hydrophobic packing of the residues

37 Theoretical results showed the presence of hydrogen bonding and intercalation in the minor groove o

38 control element that promotes intramolecular hydrogen bonding and leads to macrocycles with conformat

39 C-mannoses can be involved in intramolecular hydrogen bonding and limit the flexibility of the TSR tr

40 perturbation caused by the AraC via specific hydrogen bonding and maintain a reaction-ready active si

41 conformation (including disruption of strong hydrogen bonding and novel conformer formation) and any

42 erences in buried surface area upon binding, hydrogen bonding and other directional interactions with

43 class of drugs is incorporated possibly via hydrogen bonding and pi-pi interactions with the PcBOx s

44 ribed the competition and transition between hydrogen bonding and protonation of alkynes connected, o

45 Due to multiple, strong hydrogen bonding and salt bridge effects, CP/Ad-SS-GD we

46 nformational change driven by the collective hydrogen bonding and the sequence-mandated topology of t

47 e of HIV-1 protease inhibitors by optimizing hydrogen bonding and van der Waals interactions with the

48 Amide NH...O=C hydrogen bonding and various pai-system interactions hav

49 olecular simulations to demonstrate that the hydrogen-bonding and hydrophobic groups at the ice-bindi

50 These examples suggest that both hydrogen-bonding and stacking interactions can result in

51 Hydrogen-bonding and van der Waals interactions mediatin

52 synergistic combination of a chemical force (hydrogen bonding) and magnetic dipole coupling to assemb

53 (pai-pai and/or hydrophobic), sp(2)O-sp(2)N (hydrogen bonding) and sp(3)C-sp(2)C (CH-pai and/or hydro

54 h factors such as surface area/volume ratio, hydrogen bonding, and electrostatic interaction between

55 to form new intramolecular or intermolecular hydrogen bonding, and improve the thermal behavior and c

56 on of halogen bonding, intra-/intermolecular hydrogen bonding, and intermolecular hydrophobic interac

57 roperties owing to additional electrostatic, hydrogen-bonding, and steric interactions.

58 nating counteranions can be rescued by using hydrogen-bonding anion binders that attenuate deleteriou

59 exhibits the energetically favourable l2-l2 hydrogen-bonding arrangement, which is unprecedented for

60 m carbamate with different conformations and hydrogen bonding arrangements were ascertained using den

61 d by subtle structural deviations from ideal hydrogen-bonding arrangements or disrupted pai-stacking

62 bic layers, but with substantially different hydrogen-bonding arrangements.

63 ole nitrogen atom to participate in [NHN](+) hydrogen bonding as a proton acceptor.

64 Intra- and intermolecular hydrogen bonding as well as electrostatic interactions i

65 t a high degree of inter- and intramolecular hydrogen bonding, as well as the dendritic architecture,

66 d from the interface is attributed to strong hydrogen bonding associations between the water molecule

67 e of FRET mechanism is due to intermolecular hydrogen bonding between ADD and AA, which was confirmed

68 inal anions on the metal clusters results in hydrogen bonding between adjacent nets in the interpenet

69 PI(4,5)P(2) is stabilized by hydrogen bonding between amino acid side chains and phos

70 differences in the levels of intramolecular hydrogen bonding between each of the cyclosporins.

71 stretching vibrations allude to significant hydrogen bonding between MA and the water molecules.

72 lent solubility of NOB induced by multipoint hydrogen bonding between NOB and CAGE.

73 Hydrogen bonding between ritonavir and SBA-15 surface si

74 transform infrared analysis showed increased hydrogen bonding between SE and alginates, confirming th

75 rtial agonist salmeterol depends on specific hydrogen bonding between Ser(5.46) and Asn(6.55), and th

76 -conjugated crosslinking molecules is due to hydrogen bonding between the -B(OH)(2) terminal group of

77 o POP-pNH(2) -Py owing to the intramolecular hydrogen bonding between the amino group and coordinated

78 n ESAT-6 and beta2M in addition to the vital hydrogen bonding between the aspartate residue (Asp53) o

79 n (GFP) is known to be heavily influenced by hydrogen bonding between the core fluorophore and the su

80 rg269 undergoing an SD-dependent flipping of hydrogen bonding between the first and fifth phosphate g

81 zH(+) cations and strips featuring extensive hydrogen bonding between the Hsq(-) anions and water mol

82 the importance of charge interactions and/or hydrogen bonding between the pharmacophore and carbon su

83 ling stabilization effects of intermolecular hydrogen bonding between the side-chain functionalities

84 ies show that charge-charge interactions and hydrogen bonding between the suramin sulfonated groups a

85 We show that Ca(2+) alters hydrogen bonding between water and lipid headgroups by f

86 llective influence of aromatic interactions, hydrogen bonding, bidentate tethering, and structural ri

87 The addition of ancillary groups (e.g., hydrogen bonding, Bronsted acid/base) near the active si

88 External perturbations such as pH and hydrogen bonding can also trigger the spin state transit

89 calculations demonstrate that intramolecular hydrogen bonding can stabilize Boat, whereas electron re

90 r greater molecular elaboration and enhanced hydrogen bonding capabilities.

91 conventional 3,6-cycoladdition, the enhanced hydrogen bonding capability of HFIP uniquely results in

92 y comparison to control structures that lack hydrogen bonding capability, resulting in lower surface

93 Due to reduced hydrogen-bonding capability caused by (oxo)G, a loss of

94 a more rigid chiral environment and enhanced hydrogen-bonding capability.

95 of a heterocyclic azadiene cycloaddition by hydrogen bonding catalysis but also the first to alter t

96 de bonds, which may be expected to inhibit a hydrogen-bonding catalyst.

97 The design involves incorporation of "triple hydrogen bonding clusters" (THBCs) as side groups into t

98 Our results reveal generic backbone-backbone hydrogen bonding constraints as a determining factor in

99 of a gold ion to act as a proton acceptor in hydrogen bonding continues to remain an open question.

100 sent theoretical calculations to predict how hydrogen bonding could influence the excited states of t

101 predictions but also quantifies stacking and hydrogen bonding differences between modified NNs and th

102 In the pai-pai stacking and hydrogen-bonding directions, the intrinsic, short-range

103 esidue Ile(105) for a serine, located within hydrogen-bonding distance to Asp(22), would change the m

104 e find that organic molecules' low number of hydrogen-bonding donors and small topological polar surf

105 onal C-X...X-C/C-X...pai halogen bonding and hydrogen bonding driven crystalline architectures based

106 olvent-ion correlations, and the interfacial hydrogen bonding environment.

107 w the interplay between PCET rate constants, hydrogen-bonding equilibria, and rate-driving force rela

108 ocation of the macrocycle is controlled by a hydrogen-bonding equilibrium between the stations.

109 ribed for simultaneously extracting both the hydrogen-bonding equilibrium constants and the rate cons

110 )) Lewis acid adduct involving ferryl O-atom hydrogen-bonding, F(8)Cmpd-II(LutH(+)).

111 base triples (five) were designed, and their hydrogen bonding feasibility was confirmed by ab initio

112 Intramolecular hydrogen bonding formed by 1,10-diamide substitution sta

113 The hydrogen bonding from the pendant phenol group to Fe(III

114 A cuprous chelate bearing a secondary sphere hydrogen bonding functionality, [(PV-tmpa)Cu(I)](+), tra

115 e existence of various imidazolium-imidazole hydrogen-bonding geometries in the histidine tetrad at l

116 gh changes to the polymer spacer between the hydrogen bonding groups and the nanoparticles' surface.

117 stimate the capacity of which intramolecular hydrogen bonding has upon restricting the E/Z isomerizat

118 incrementally to a nonconventional OH...pai hydrogen bonding (HB) interaction.

119 hodologies utilizing XB remain rare, and the hydrogen-bonding (HB) catalysis congeners are more wides

120 The meta-amino GFPc exhibits hydrogen-bonding (HB) mediated fluorescence quenching, a

121 of AnH(2)Q with a ratio of 13 (298 K) in non-hydrogen-bonding (HB) solvents, but the reactivity towar

122 ld, in comparison to the halogen bonding and hydrogen bonding heteroditopic receptor analogues.

123 rdinated or noncoordinated to phenol through hydrogen bonding in a dichloromethane solution, the rate

124 Hydrogen bonding in addition to electrostatic interactio

125 resent results suggest that gold-ion-induced hydrogen bonding in an actual solvent environment may be

126 AIE-active aggregates through intermolecular hydrogen bonding in aqueous media.

127 xhibited an increase, indicating the role of hydrogen bonding in enhancing the photocatalysis for CO(

128 We characterize the double-faced nature of hydrogen bonding in hydroxy-functionalized ionic liquids

129 t the TM helix conformation and the backbone hydrogen bonding in lipid bilayers differ from the micel

130 lectron aromatic system, suggesting that the hydrogen bonding in salts 3H(+)BF(4)(-)-6H(+)BF(4)(-) re

131 dine ligands, highlighting the importance of hydrogen bonding in templating the cubane assembly.

132 de dihedral angles accompanying transannular hydrogen bonding in the [3.3]paracyclophane and (b) mono

133 eavage state to reach out for water-mediated hydrogen bonding in the cyclophosphate product.

134 mputational data indicate that second-sphere hydrogen bonding induces structural distortion of the [C

135 e interplay of chiral, chelate, solvent, and hydrogen-bonding information in the self-assembly of a s

136 the morpholine oxygen, both forming the key hydrogen bonding interaction and conveying selectivity o

137 The potential hydrogen bonding interaction with Thr599 in the pocket w

138 D3 active site, Asn(255) engages in a unique hydrogen-bonding interaction with the target histidine o

139 on coefficients further support this unusual hydrogen-bonding interaction.

140 improved unimer solvation by a reduction of hydrogen bonding interactions among PLLA chains.

141 or the first time for Ln(III) ion complexes, hydrogen bonding interactions and pai-pai stacking suppo

142 ociate into anti-electrostatic oligomers via hydrogen bonding interactions at millimolar concentratio

143 erization of a series of iron complexes with hydrogen bonding interactions between bound aquo or hydr

144 Herein, we investigate the role of hydrogen bonding interactions induced when metal halide

145 A mechanism is proposed for how key hydrogen bonding interactions might affect the hydricity

146 protease-inhibitor complexes revealed strong hydrogen bonding interactions of both (R)- and (S)-stere

147 Hydrogen bonding interactions of Glu200 with residues co

148 a combination of hydrophobic and inter-lipid hydrogen bonding interactions to stabilize bacterial mem

149 p was involved in a unique pattern of direct hydrogen bonding interactions with the backbone amides o

150 Furthermore, G40 can also establish hydrogen bonding interactions with the nonbridging oxyge

151 remaining inner-sphere water molecules make hydrogen bonding interactions with the RNA.

152 nium carbamate chains that are stabilized by hydrogen bonding interactions within the framework pores

153 regation phenomenon through pai-stacking and hydrogen bonding interactions, asphaltene aggregates can

154 the large changes in mobility, affinity for hydrogen bonding interactions, etc., that are reflected

155 igid and nonconjugated) or by supramolecular hydrogen bonding interactions.

156 nd the MOF host through pai-pai stacking and hydrogen bonding interactions.

157 uations of interfacial water, as well as the hydrogen-bonding interactions and conformational motions

158 hat boronic acid activation proceeds through hydrogen-bonding interactions and not coordination with

159 g molecule-based crystal structures in which hydrogen-bonding interactions are intentionally partitio

160 The hydrogen-bonding interactions are the reason for the imp

161 en-bonding analyses suggest the formation of hydrogen-bonding interactions between the flavin and Arg

162 rkedly, this ultralow detection is driven by hydrogen-bonding interactions between the linker and the

163 s of the catalyst or photosensitizer, but to hydrogen-bonding interactions between them.

164 bond to Y(32), as well as the possibility of hydrogen-bonding interactions between Y(32) and E(13), t

165 d to unfluorinated analogues wherein NH...OC hydrogen-bonding interactions force benzamide and naphth

166 a terminal Fe(III)-oxo center stabilized by hydrogen-bonding interactions from pendant ( tert-butyla

167 Hydrogen-bonding interactions have been explored in cata

168 Binding and catalysis are facilitated by hydrogen-bonding interactions in a hydrophobic pocket.

169 e conformational flexibility of Y731 and the hydrogen-bonding interactions of both Y731 and Y356 with

170 Their inhibitory efficacy is based on the hydrogen-bonding interactions of the carbonyl oxygen and

171 hotocatalytic performance by introduction of hydrogen-bonding interactions to a Re bipyridine catalys

172 e noncanonical binding motif, but with fewer hydrogen-bonding interactions to the protein than is obs

173 Y356 and Y731 exhibit hydrogen-bonding interactions with interfacial water mol

174 -naphthyl)ethylammonium and their asymmetric hydrogen-bonding interactions with lead bromide-based la

175 O(2) capture in 2-ampd-Mg(2)(dobpdc) through hydrogen-bonding interactions with the carbamate groups

176 te involves a folded conformation due to the hydrogen-bonding interactions with the hydroxyl groups o

177 has been predominantly limited to exploiting hydrogen-bonding interactions, while the relevant atomic

178 ze the H(3)PO(4) network in the channels via hydrogen-bonding interactions.

179 Hydrogen bonding is a key governing force in molecular r

180 The following major results are obtained: Hydrogen bonding is clearly shown to weaken at elevated

181 e (AMP) during incorporation, this base pair hydrogen bonding is not sufficient to hold an ATP substr

182 Additionally, a limiting case of hydrogen bonding is observed when the benzamide derivati

183 Complex hydrogen bonding is postulated as the root cause of thei

184 ter in various phases potentially reveal how hydrogen bonding is reflected in the condensed phase ele

185 netics of this process are attributable to a hydrogen bonding-like interaction between the agostic C-

186 The SEI model oversimplifies the hydrogen-bonding mechanisms by viewing them as interacti

187 ltiple types of supramolecular interactions (hydrogen bonding, metal complexation, and dynamic covale

188 fective, intermolecular interactions such as hydrogen bonding, metal-ligand coordination, and the hyd

189 ross-linking (e.g., guest-host interactions, hydrogen bonding, metal-ligand coordination, grafted bio

190 01 angstrom or less, even in the presence of hydrogen bonding, metal-metal bonding, and electrostatic

191 featuring conjugated backbone decorated with hydrogen-bonding moieties distinct from common organic s

192 th and without secondary-coordination-sphere hydrogen-bonding moieties, was studied at -135 degrees C

193 udies revealed that the substrates require a hydrogen-bonding moiety for selectivity.

194 valent (ester bond) and non-covalent (strong hydrogen-bonding, mostly) interactions.

195 mechanical force is applied, exposing their hydrogen bonding motifs and therefore making the membran

196 t of halogenated compounds expressing paired hydrogen-bonding motifs, termed FragLites.

197 Herein, we highlight that non-classical hydrogen bonding (NCHB), likely resulting from hyperconj

198 lso carried out to assess differences in the hydrogen-bonding net between sialyl donors.

199 precise domain arrangement and complementary hydrogen bonding network defines the subunit arrangement

200 dimer-dimer interface requires an intricate hydrogen bonding network involving residues R491 and D58

201 ed to GTP binding originates in the backbone hydrogen bonding network of EF-Tu.

202 r can be triggered by point-mutations in the hydrogen bonding network that controls the selectivity f

203 ma ligand-binding domain revealed an altered hydrogen bonding network, including the formation of wat

204 angement that is stabilized by an N-terminal hydrogen bonding network.

205 ntinuous template strand are stabilized by a hydrogen bonding network.

206 o acids and water molecules as well as their hydrogen bonding network.

207 eviously, residues were identified forming a hydrogen-bonding network between active site cofactor an

208 Extensive hydrophobic interactions and a hydrogen-bonding network between the protein and Diprovo

209 The Ca(2+)-facilitated hydrogen-bonding network forms the structural basis of t

210 Protonation of Ci1 leads to a rigid hydrogen-bonding network in the active-site region.

211 ikely drove additional changes in a delicate hydrogen-bonding network that further stabilized S1-S3 s

212 rongly influences both the protein and water hydrogen-bonding network throughout the channel, providi

213 ere it then uses an arginine/lysine-mediated hydrogen-bonding network to reposition the asparagine in

214 einhardtii evaluating dynamic changes in the hydrogen-bonding network upon photoreduction.

215 tituting molecular moieties, its fluctuating hydrogen-bonding network, as well as pair-correlation fu

216 f water are driven by alterations to water's hydrogen-bonding network-influenced by water interaction

217 s, partially due to the lack of a consistent hydrogen-bonding network.

218 e is distorted when embedded in its extended hydrogen-bonding network.

219 protonation of His144 and reorganization of hydrogen bonding networks in RopB, which facilitates SIP

220 ed with IR spectroscopy to study how alkanol hydrogen-bonding networks confined within hydrophobic an

221 r amino acid residues and revealed intricate hydrogen-bonding networks in the active-site cavity and

222 riven conformational changes, water-mediated hydrogen-bonding networks tie together the converged dom

223 (1)H/(19)F NMR study to gain information on hydrogen-bonding networks with fluoride in solution, as

224 fference maps, allowing a direct analysis of hydrogen-bonding networks.

225 formation; simply removing it destroys a key hydrogen-bonding node.

226 adruplexes (G4), which are stabilized by the hydrogen bonding of guanine residues.

227 -conjugated enamines promoted by the solvent hydrogen bonding of hexafluoroisopropanol (HFIP) that is

228 Triple-helix formation, using Hoogsteen hydrogen bonding of triplex-forming oligonucleotides, re

229 the pocket of this domain is accompanied by hydrogen-bonding of the dansyl chromophore which functio

230 this band cannot be attributed to a loss of hydrogen bonding only.

231 re of the motor for recognition of different hydrogen-bonding organocatalysts a greater than 10-fold

232 monly used non-covalent interactions include hydrogen bonding, pai-pai stacking, charge transfer inte

233 We show that hydrogen bonding, pai/sp(2), and hydrophobic interaction

234 However, the hydrogen bonding partnership remains unresolved.

235 etween the cytosolic domains, and an altered hydrogen bonding pattern around residue 340.

236 ork show the emergence of the characteristic hydrogen-bonding pattern of ice I in clusters containing

237 ecular dynamics simulations indicate altered hydrogen-bonding patterns at the dimer interface, and cr

238 y distinct pai-pai-stacking modes and unique hydrogen-bonding patterns.

239 of temperatures, showing the dramatic effect hydrogen bonding perturbation on polar species.

240 Here, we demonstrate that hydrogen bonding phase-transfer catalysis with KF provid

241 his process, which highlights the ability of hydrogen bonding phase-transfer catalysts to couple two

242 chor the clathrate-like water through direct hydrogen-bonding, positioning and slowing the dynamics o

243 erine show 5hmC-specificity that mirrors the hydrogen bonding potential of the side chain (C-H < S-H

244 r involving thiourea orchestrated bifurcated hydrogen bonding proceeded in an asynchronous concerted

245 p, lowering the electrochemical barrier, and hydrogen bonding promotes the reaction that produces pol

246 water are compared with halogen bonding and hydrogen bonding receptor analogues.

247 to act as proton acceptor and participate in hydrogen bonding remains an open question.

248 substrate-bound structure and satisfies all hydrogen-bonding requirements of the ligand.

249 he antagonists bind specifically to the same hydrogen-bonding residues and induce a similar closed co

250 in structural behavior follows directly from hydrogen-bonding restrictions and suggests that the prot

251 SO interacted with protein isolates through hydrogen bonding resulted a strong network structure of

252 ict E/Z isomerization through intramolecular hydrogen bonding, resulting in mild to moderately fluore

253 ders of magnitude greater in comparison to a hydrogen bonding rotaxane host analogue.

254 the participation of Glu-818 in an intricate hydrogen-bonding/salt-bridge network, connecting it to k

255 dopted in the beta polymorph facilitate this hydrogen-bonding scheme while avoiding steric conflict o

256 re characterized by different intramolecular hydrogen bonding schemes that arise largely from differe

257 methanoisoindol-1-one scaffold with a lactam hydrogen-bonding site.

258 In particular, moderate-strength hydrogen bonding stabilizes a cobalt(III)-superoxo speci

259 andscape defined by beta-sheet alignment and hydrogen-bonding states, whereas transitions involving s

260 depend strongly on the secondary structure (hydrogen bonding status) of the oligonucleotides, but ne

261 ent of water in hydrophobic pores alters its hydrogen bonding structure and related properties such a

262 pore size modifications as well as the water hydrogen bonding structure based on detailed infrared sp

263 of information on exact proton locations and hydrogen bonding structures in a bona fide metalloenzyme

264 olidinyl)-1,4-benzodioxanes bearing a small, hydrogen-bonding substituent at the 7-, 6-, or 5-positio

265 mal titration calorimetry, and involved more hydrogen bonding than hydrophobic interactions in the ca

266 ding of cellulose, including the key role of hydrogen bonding, the dependence of structural interface

267 transformed Au-NP surfaces to create strong hydrogen bonding through adsorbed oxyanions with soil su

268 d with a second water molecule stabilized by hydrogen bonding to a Gln side chain in the active site,

269 and computational analysis of the effects of hydrogen bonding to a metal dinitrogen complex.

270 rea-galabiose binding, suggesting additional hydrogen bonding to terminal GalNAc of Gb4 and the urea

271 c center substituted with a group capable of hydrogen bonding to the catalyst are demonstrated.

272 nitially water decorates the metal channels, hydrogen bonding to the exposed O ligands that bind bita

273 s and orients the imine to hydride attack by hydrogen bonding to the PO or SO group on the imine nitr

274 essed in solvents that are unable to provide hydrogen bonding to the second-sphere N-H groups.

275 y establish the identity of gold-ion-induced hydrogen bonding via experimental techniques.

276 ward the reaction revealed that nonclassical hydrogen bonding was involved in the stabilization of th

277 Eventually, the concept of lactam hydrogen bonding was transferred to transition-metal cat

278 thermodynamic parameters, van der Waals and hydrogen bonding were found to have important roles in b

279 ins with CBB G-250 dye, primarily related to hydrogen bonding, were confirmed by capillary zone elect

280 tage is that the footprint reflects SASA and hydrogen bonding, whereas one drawback is the labeling i

281 hts the crucial roles of charge capacity and hydrogen bonding, which can help elucidate the mechanism

282 duced efficacy, likely due to the absence of hydrogen bonding with a conserved asparagine residue at

283 was attributed to the strong interaction (by hydrogen bonding with AOT anion and ion-dipole interacti

284 guest molecules gain stability through OH O hydrogen bonding with beta-CD and are well shielded in t

285 specific DNA-binding proteins show balanced hydrogen bonding with each of the two DNA strands while

286 atalyst engages two of its four NH groups in hydrogen bonding with fluoride, an arrangement that allo

287 le bonding of halogen and sulfur atoms, weak hydrogen bonding with fluorine as acceptor, and differen

288 anic molecules in aqueous media by combining hydrogen bonding with hydrophobic interactions.

289 t interfacial water orientations and prevent hydrogen bonding with lipid ester carbonyls.

290 selecting a single conformation by blocking hydrogen bonding with photolabile protection groups.

291 les on the Zr(6) nodes, which are capable of hydrogen bonding with polar functional groups of guest m

292 e, mutation of the G4 motif, responsible for hydrogen bonding with the guanine base, abolished the GT

293 romotes new modes of guest encapsulation via hydrogen bonding with the pai systems of the unsaturated

294 l for high potency, likely because of strong hydrogen bonding with the RNA backbone of C2469, as sugg

295 mediate, and Arg-56 facilitates catalysis by hydrogen bonding with the sulfhydryl of Cys-aldimine.

296 that the D-amino acid cannot participate in hydrogen-bonding with the P-site tRNA that is required f

297 w that the charge capacity (of the site) and hydrogen bonding (with the intermediates), which were ne

298 different ligands impacts upon the degree of hydrogen-bonding within the assembly, stabilizing specif

299 4WJ-like motif through pai-pai stacking and hydrogen bonding, without forming any platinum-nitrogen

300 Selection for hydrogen bonding yields a preponderance of L or D amino