ライフサイエンスコーパス: hydrogen bonding

1 CdTe QDs induced the aggregation of QDs via hydrogen bonding.

2 FeH) unit to the protein environment through hydrogen bonding.

3 ent, E, is H, and we can have strong or weak hydrogen bonding.

4 a crystalline carbonate salt by guanidinium hydrogen bonding.

5 lizing reactive intermediates with [C-H...N]-hydrogen bonding.

6 sugar binding in all GLUT1 conformations via hydrogen bonding.

7 activation towards electron transfer through hydrogen bonding.

8 ch must be more than compensated by enhanced hydrogen bonding.

9 a geometry better-suited for intramolecular hydrogen bonding.

10 nucleophile binds to the thiourea moiety by hydrogen bonding.

11 instead with precursor complex formation by hydrogen bonding.

12 roscopy we probe changes in conformation and hydrogen bonding.

13 nitrate, bicarbonate and sulfate anions via hydrogen bonding.

14 ers, each of which is stabilized by in-plane hydrogen bonding.

15 T photocycloaddition using TADDOLs as chiral hydrogen-bonding additives provided access to (+)-foveog

16 The interligand hydrogen bonding also allows site-selectivity to be harn

17 interacted with anthocyanins mainly through hydrogen bonding, although some hydrophobic interaction

18 In contrast to the case of hydrogen bonding among solvent water molecules, we find

19 analysis indicated weak interactions through hydrogen bonding among starch granules, RB powder and PD

20 Comparisons with control species or solely hydrogen-bonding analogues reveal unique characteristics

21 As cyanide is capable of various kinds of hydrogen bonding and as it is a quite strong sterically

22 der to probe the interplay between sidechain hydrogen bonding and backbone conformational preferences

23 ther bilayer properties, such as interfacial hydrogen bonding and bilayer permeability.

24 structures are based on G-quartets formed by hydrogen bonding and cation-coordination of guanosines.

25 The observations suggest decreased RNA hydrogen bonding and changed RNA conformation upon IRP1

26 competing reaction pathways, both [C-H...O]-hydrogen bonding and electrophile preorganization by coo

27 with volumes ranging from 35 to 219 A(3) via hydrogen bonding and electrostatic interactions.

28 well as more exotic interactions such as C-H hydrogen bonding and halogen bonding.

29 PP fibrils and demonstrate the importance of hydrogen bonding and hydrophobic interactions in the oli

30 le a great deal of knowledge on the roles of hydrogen bonding and hydrophobicity in proteins have res

31 rth-East sugar pucker, due to intramolecular hydrogen bonding and hyperconjugation effects.

32 and reveals a significant contribution from hydrogen bonding and interaction with K(+).

33 ir interaction with gliadins is dominated by hydrogen bonding and is relatively weaker.

34 Here we report a targeted modification of hydrogen bonding and its effect on guest binding in redo

35 It is concluded that hydrogen bonding and local electrostatics protect the re

36 Hydrogen bonding and non-bonded interaction energies, an

37 yl oxidant in a specific orientation through hydrogen bonding and pi-stacking interactions.

38 Competition between hydrogen bonding and proton transfer reactions was studi

39 sensitive in distinguishing between backbone hydrogen bonding and side-chain or water-mediated hydrog

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

41 amides and amidines led to the influence of hydrogen bonding and to NMR methods for chemical kinetic

42 These values showed that hydrogen bonding and van der Waals forces were the main

43 prevents strong mixing between orbitals upon hydrogen bonding and, thus, inhibits substantial charge

44 ere is no experimental evidence for enhanced hydrogen bonding and/or icebergs in such solutions.

45 Hydrogen-bonding and clustering phenomena in trehalose s

46 te the intermediate iminium cation by P=OH-O hydrogen-bonding and NH-C electrostatic interactions.

47 ree energy components include van der Waals, hydrogen bonding, and dipole interactions; side-chain co

48 hyltransferases may be mwedgeodulated by CHO hydrogen bonding, and factors other than axial compressi

49 was prepared and their druglike properties, hydrogen bonding, and lipophilicity were studied.

50 illing hydrogel into the damage site, strong hydrogen bonding, and molecular interdiffusion.

51 hese factors include Coulombic interactions, hydrogen bonding, and solvation, as well as backbone mot

52 packing forces, as opposed to complementary hydrogen bonding, and while they are both retained withi

53 sphere interactions, substituents capable of hydrogen bonding are included as pyrazolates with arylam

54 nzoate where the halogen bonding and C-H...O hydrogen bonding are well-matched.

55 ter as the critical element for the enhanced hydrogen bonding around a hydrophobic solute.

56 e to shape a cavity closed by a four-fold OH-hydrogen-bonding array, form a highly ordered porous net

57 urthermore, this capping mechanism, based on hydrogen bonding as explained by ab initio modelling, op

58 ctional halogen bonding and halogen-directed hydrogen bonding as follows: favorable electrostatic int

59 ur results highlight the vital importance of hydrogen bonding at desolvated interfaces, providing a n

60 Hydrogen bonding at the indole amine most likely stabili

61 aracteristics of communication-module bases: hydrogen bonding, base stacking, and distance to the enz

62 Despite hydrogen bonding being the dominant interaction, precise

63 studies on C1C2, no direct or water-mediated hydrogen bonding between an aspartate and a cysteine (D1

64 xoG phosphate group (PO4) interfere with the hydrogen bonding between Asp192 and Arg258, whose rotati

65 ormation is stabilized by the intermolecular hydrogen bonding between C horizontal lineO...HN with an

66 NMR studies reveal the presence of hydrogen bonding between HFIP and a pyrimidine nitrogen

67 olled by the N2 functionality because of the hydrogen bonding between N2 and O4.

68 FTIR also proposed hydrogen bonding between niosomes and proteins.

69 dimensional shapes, guided by the pattern of hydrogen bonding between nucleotides.

70 showed electrostatic interactions as well as hydrogen bonding between phospholipid head groups and am

71 stained by orthogonal metal coordination and hydrogen bonding between telechelic polymers that featur

72 lly restricted states through intramolecular hydrogen bonding between the amide and imide groups.

73 Further, potentiometric studies suggest that hydrogen bonding between the guest anions and the amide/

74 that was associated with the intermolecular hydrogen bonding between the hydroxyl groups of QC and P

75 Evidence of hydrogen bonding between the N-H group of nifedipine and

76 98 K and 1 bar (6.0 mmol g(-1)) and involves hydrogen bonding between the OH group of the host and th

77 ropose a "step in" mechanism, which involves hydrogen bonding between water and the DMSO aggregate sp

78 acking, the hydrophobic effect, and possible hydrogen-bonding between pigment and copigment) and of s

79 horizontal lineN imido bond through initial hydrogen-bonding between X-OH and the N-atom of 3 to for

80 c "icebergs" arising from strengthened water hydrogen bonding, but there is no experimental evidence

81 w that supramolecular networks stabilised by hydrogen bonding can be formed on BP, and that these mon

82 lts demonstrate that interactions other than hydrogen bonding can contribute to every step of informa

83 example, [methylpi] coordination and [C-HO] hydrogen bonding-can readily invert the relative thermod

84 By providing additional hydrogen-bonding capacity, the Pro-->2-Hyp conversion al

85 und to be competitive with the corresponding hydrogen bonding catalysis reported in literature.

86 ols and (thio)ureas, typically classified as hydrogen bonding catalysts, as well as stronger phosphor

87 1,3-Disiloxanediols are effective hydrogen-bonding catalysts that exhibit enhanced activit

88 M and supramolecular cation, featuring short hydrogen-bonding contacts between the electron-poor POM

89 ) anions are higher than those found for the hydrogen-bonding counterpart.

90 ing interactions relative to their normal OH hydrogen bonding counterparts.

91 Despite the fundamental importance of hydrogen bonding, dependence on this stabilizing force p

92 mino acids of the two proteins positioned at hydrogen-bonding distances from each other.

93 atson-Crick base pairing but have rearranged hydrogen bonding donor and acceptor groups.

94 ure-induced aggregation was caused mainly by hydrogen bonding during pressurisation and not hydrophob

95 amined how regio-specific methylation at the hydrogen bonding edge of adenine and guanine in mRNA aff

96 ected complexes with respect to ion pairing, hydrogen bonding, electrostatic contributions, halogen b

97 ion was found among hydrogen exchange rates, hydrogen bonding energies, and amino acid solvent-access

98 very strong tendency for aggregation due to hydrogen bonding, especially to form homodimers as seen

99 s, including density, dielectric properties, hydrogen bonding, etc.

100 e presence of bifurcated weak intramolecular hydrogen bonding (F...HN) and N(+)...F(delta-) charge-di

101 n addition to electrostatic interactions and hydrogen bonding, [Fe(bisDHBS)](2-) binds through coordi

102 (L99A/M102Q), Gln102 horizontal lineO...H-N hydrogen bonding for Ab and BEtAb was observed in the cr

103 The importance of hydrogen bonding for this unusual regioselectivity could

104 1,3 fashion to the fully reduced state, with hydrogen bonding from Lys397, and two electrons are tran

105 -63 carboxamide by Arg85' to preclude direct hydrogen bonding from water to the target gamma-PO3(-) g

106 Hydrogen-bonding from MeOH is critical for the hyponitri

107 namely van der Waals (vdW), pi-stacking, and hydrogen bonding groups.

108 e azobenzene tether functionalized with urea hydrogen-bonding groups and d-carbohydrates as chiral se

109 ent for quinones that feature intramolecular hydrogen bonding, halogen substituents, charged substitu

110 ally electrostatic interactions, but whereas hydrogen bonding has a well-documented record of stabili

111 ette, favored by a network of intermolecular hydrogen bonding, has been proposed.

112 nt bonding (HVB), secondary bonding (SB) and hydrogen bonding (HB) a nucleophilic and an electrophili

113 Both hydrogen bonding (HB) and halogen bonding (XB) are essen

114 bond in Shaker potassium channels with a non-hydrogen bonding homologue of tryptophan, Ind.

115 cetamidopyridinyl)isophthalamide-barbiturate hydrogen-bonding host-guest complexes are separately inc

116 and biochemical systems (London dispersion, hydrogen bonding, hydrophobic, and electrostatic), and i

117 side arms with central 2-bromoimidazolium or hydrogen-bonding imidazolium receptors.

118 us ev-idence for the key 1D driving force of hydrogen bonding in enhancing the persistency of monomer

119 abilization of organic radical anions by C-H hydrogen bonding in pi-stacked pairs of cyanostar macroc

120 n with OSM, suggesting an important role for hydrogen bonding in stabilizing sterol/SM interactions.

121 1 degrees C gives insight into the extent of hydrogen bonding in supercritical water.

122 led N3 and N1, that differ in the pattern of hydrogen bonding in the core.

123 s in a reversal of the directionality of the hydrogen bonding in the helix.

124 Besides hydrogen bonding in the major groove (base readout), pro

125 neutral amides with [AuCl4 ](-) ions through hydrogen bonding in the organic phase, as shown by EXAFS

126 ct evidence for Watson-Crick (G)N2H2...O2(T) hydrogen bonding in the transient tautomeric state.

127 The nature and extent of hydrogen bonding in water has been scrutinized for decad

128 ster in the molecular-level understanding of hydrogen bonding in water.

129 t is stabilized by intra- and intermolecular hydrogen bonding, including an extended beta-sheet struc

130 that this selectivity is the result of a key hydrogen bonding interaction between the substrate and c

131 ion, while the benzonitrile group accepts a hydrogen-bonding interaction from the side chain residue

132 dies have suggested the extended CD-loop and hydrogen-bonding interaction network within the ZIKV env

133 nanodroplet, BOMD simulation shows that the hydrogen-bonding interaction of (SO2)O...H(H2O) becomes

134 ic influence combined with a weak allosteric hydrogen-bonding interaction that significantly lowers t

135 An interesting substrate-solvent hydrogen-bonding interaction was observed.

136 ding via O6 coordination, and 3) binding via hydrogen-bonding interaction with the first-shell water

137 The crystal structure shows that the hydrogen bonding interactions between pairs of 3 result

138 erryl intermediates are finely tuned through hydrogen bonding interactions between proximal ligands a

139 xane 3 subsetCBPQT(4+) reveal that [C-H...O] hydrogen bonding interactions between the acidic alpha-H

140 s showed very similar geometric features and hydrogen bonding interactions for the characterized stat

141 revealed the critical synergy of halogen and hydrogen bonding interactions in anion discrimination.

142 onation at the flavin N5 position alters the hydrogen bonding interactions of an invariant Gln residu

143 eory, reveals the distinctive nature of CF2H hydrogen bonding interactions relative to their normal O

144 obing, suggested that resulting intraluminal hydrogen bonding interactions stabilize the open-channel

145 ystal structure reveals a pi-pi stacking and hydrogen bonding interactions that stabilize the new pro

146 w for the direct detection of intermolecular hydrogen bonding interactions through the lengthening of

147 2-5 subsetCBPQT(4+) are engaged in [C-H...O] hydrogen bonding interactions with CBPQT(4+), whereas th

148 ts suggest that an amide can mimic important hydrogen bonding interactions with proteins required for

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

150 in conformation allow the amide to establish hydrogen bonding interactions with the protein.

151 A network of AQP4 loop D hydrogen bonding interactions, identified using molecula

152 arginine side chain in AAV2-R432A eliminated hydrogen bonding interactions, resulting in altered intr

153 aine-H 2 O dimers or complexes with enhanced hydrogen bonding interactions.

154 g with some van der Waals, electrostatic and hydrogen bonding interactions.

155 transition states (TDTSs) via strong N-H...O hydrogen-bonding interactions (HBIs).

156 the gem-dinitro carbon results in extensive hydrogen-bonding interactions and higher packing coeffic

157 priate counteranion driven ion-pair-assisted hydrogen-bonding interactions are found responsible for

158 These results have shown that a variety of hydrogen-bonding interactions are important in determini

159 stabilization is provided by intermolecular hydrogen-bonding interactions between acidic positions o

160 de observable by incorporating second-sphere hydrogen-bonding interactions between bound H2 O2 and th

161 ighly optimized and symmetric intermolecular hydrogen-bonding interactions between the main building

162 Substrate scope investigations suggest that hydrogen-bonding interactions between the oxygen in the

163 ulfide anion, HS(-) , using only reversible, hydrogen-bonding interactions in a series of bis(ethynyl

164 These hydrogen-bonding interactions likely result from stereoc

165 for the polymerization step is regulated by hydrogen-bonding interactions made between the incoming

166 cognition and signaling, we investigated the hydrogen-bonding interactions of the iron-bound CO and N

167 th ab initio molecular dynamics simulations, hydrogen-bonding interactions of two key principal amine

168 In particular, hydrogen-bonding interactions through carbamate groups w

169 The use of hydrogen-bonding interactions to direct the noncovalent

170 In contrast, hydrogen-bonding interactions within and with the protea

171 irected inwards and anchored by stacking and hydrogen-bonding interactions.

172 unique bioinspired environment with multiple hydrogen-bonding interactions.

173 in (LBD) via a mix of positively charged and hydrogen-bonding interactions.

174 te effects such as the role of Coulombic and hydrogen-bonding interactions.

175 rough cooperative steric, electrostatic, and hydrogen-bonding interactions.

176 in the gas phase due to strong Coulombic and hydrogen-bonding interactions.

177 rative non-covalent (pi-pi, solvophobic, and hydrogen bonding) interactions.

178 ce of a number of the intramolecular C-H...S hydrogen bonding, intermolecular C-H...S, C-H...Cl, and

179 substitutions at Gly77 and Tyr78 perturb the hydrogen bonding involving the buried water molecules st

180 The lack of hydrogen bonding involving the C12OH group of the steroi

181 anonical noncovalent interactions, including hydrogen bonding, ion pairing, and pi stacking, have bec

182 The simulations indicated hydrogen bonding is a key component leading to propofol-

183 uster, including supramolecular assembly via hydrogen bonding is detailed via small-angle X-ray scatt

184 Hydrogen bonding is discussed in the context of medicina

185 The results show that hydrogen bonding is important for sterol/SM and ceramide

186 The bisulfate dimer's OHO hydrogen bonding is seen in a (1) H NMR peak at 13.75 pp

187 lts demonstrate that even in the presence of hydrogen bonding it is possible to relate nitrile absorp

188 mpler liquids, water's orientation-dependent hydrogen bonding leads to open tetrahedral cage-like str

189 The role of hydrogen bonding led us to the rotation of NH4(+) within

190 ond-type binding interactions and two weakly hydrogen-bonding-like binding interactions).

191 presents new clues to the mechanism by which hydrogen bonding maintains global structural integrity.

192 The combination of binding forces, including hydrogen bonding, metal coordination, and dynamic hydraz

193 gen bonding and side-chain or water-mediated hydrogen bonding might be needed in the reduction of Coi

194 ored over Wynberg's widely accepted ion pair-hydrogen bonding model and represent the first detailed

195 howed that Houk's bifunctional Bronsted acid-hydrogen bonding model, which works for cinchonidine or

196 Fundamentally, this study shows that small hydrogen-bonding molecules can be used to induce the ass

197 ably due to the co-operative geometry of the hydrogen bonding motif.

198 e hemiaminal intermediate is arrested by the hydrogen-bonding motif to yield benzoxazinone.

199 t in other flaviviruses, organizes a central hydrogen bonding network at NS1 dimer interface.

200 protocol utilizes iterative optimization of hydrogen bonding network combined with atomic-level ener

201 sive hydrophobic interactions and the unique hydrogen bonding network contribute to the great potency

202 It is shown that mutations where the hydrogen bonding network that involves the Tyr140 and Tr

203 ydrophobic elements, along with an elaborate hydrogen bonding network that is mediated by sodium ion.

204 the creation of a stabilizing intramolecular hydrogen bonding network.

205 ZIKV recombinant viruses that disrupted the hydrogen-bonding network (350A, 351A, and 350A/351A) or

206 es (Val-86), open channel stability, and the hydrogen-bonding network (K93I and K93N).

207 ergy terms introduced in 3DRobot improve the hydrogen-bonding network and compactness of decoys, whic

208 the basis of NOEs, and a previously unknown hydrogen-bonding network between Man3 and CV-N was disco

209 The intramolecular hydrogen-bonding network flips nearly 90 degrees , and t

210 gold cluster cores were held together by the hydrogen-bonding network formed by their capping ligands

211 inate metal center are supported through the hydrogen-bonding network in a fashion reminiscent of the

212 al data suggests that a Ser(84)-H2O-Lys(114) hydrogen-bonding network in human serine racemase lowers

213 results confirm the importance of the distal hydrogen-bonding network in ligand recognition and commu

214 iff's base triggers the rearrangement of the hydrogen-bonding network involving residues on H6 and wi

215 ystallinity reveals that La(3+) disrupts the hydrogen-bonding network of water molecules located remo

216 arkable stability may be attributable to the hydrogen-bonding network provided by the main chain of t

217 ght activation of AppA involves changes in a hydrogen-bonding network that surrounds the flavin chrom

218 Residue Y21, a component of the hydrogen-bonding network, is known to be essential for p

219 which, when replaced by His264 strengthens a hydrogen-bonding network, leading to a more stable virus

220 lies, characterized by a square or honeycomb hydrogen-bonding network, respectively.

221 e orientations, held together by an extended hydrogen-bonding network.

222 d at opposite ends of the RH1 intramolecular hydrogen-bonding network.

223 The differences between hydrogen bonding networks of cellulose surface and cryst

224 n beam to probe the effect of differences in hydrogen bonding networks on mineral solubility.

225 ossess out-of-plane hydrogen atoms that form hydrogen bonding networks which stabilize the layered st

226 ext of differences in the OH bond strengths, hydrogen bonding networks, and the presence or absence o

227 In contrast, the corresponding hydrogen-bonding networks in NMCA, SFC-1, and SME-1 carb

228 losteric ligand-binding determinant, whereas hydrogen-bonding networks within the extracellular vesti

229 pectra provide evidence for the preferential hydrogen bonding of acidic hydrogens with electron-rich

230 cleotide disrupts the phosphate backbone and hydrogen bonding of an adjacent base pair.

231 d DFT calculations, which indicate favorable hydrogen bonding of cyanide to the most acidic axial hyd

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

233 with polyaromatic surfaces, and very strong hydrogen bonding of ionizable compounds with surface fun

234 Through-space hydrogen bonding of N-Ac-VL was investigated by a two-di

235 uch cycloaddition reactions by using solvent hydrogen bonding of non-nucleophilic perfluoroalcohols,

236 These results provide a benchmark for hydrogen bonding of other nitrogen-containing acids and

237 We demonstrate that enhanced hydrogen bonding of the Asn378 side chain with the FADH(

238 Thus, the "cyanide effect" is due to dual hydrogen bonding of the axial hydroxy group which enhanc

239 formation by the cis-isomer is suppressed by hydrogen bonding of the cis-aldehyde carbonyl with the D

240 most acidic axial hydroxy group supported by hydrogen bonding of the equatorial hydroxy group to the

241 iting the heretofore unknown propensity of a hydrogen-bonding OH-arene interaction to switch to the a

242 Further understanding of the effect of hydrogen bonding on the structure and reactivity of comp

243 Three further VP24 mutations change hydrogen bonding or cause conformational changes.

244 ersible supramolecular interactions, such as hydrogen bonding or electrostatic interactions.

245 Interpolymer hydrogen bonding or metal-coordination achieves dynamic

246 piezosensors with MTs immobilized either by hydrogen bonding or thin polypyrrole (PPy) binding film.

247 Using RACER, we identified hydrogen-bonding (or base pairing), base stacking, and e

248 were correlated with perturbation of charge, hydrogen bonding, or packing, likely affecting the tempe

249 redict the pKa's of several families of dual hydrogen-bonding organocatalysts/anion receptors, includ

250 mics simulations indicate that the Trp434Ind hydrogen bonding partner, Asp447, unexpectedly 'flips ou

251 evidence for the formation of a beta-hairpin hydrogen bonding pattern.

252 For the Trpin/Metout conformation, the hydrogen-bonding pattern conducive to the proton relay i

253 resonance NMR show marked differences in the hydrogen-bonding pattern of the two enantiomers at the b

254 nd Z-rotaxanes show different intercomponent hydrogen bonding patterns.

255 his work can be generally applied to examine hydrogen-bonding patterns in nucleic acid transient stat

256 00 and 3700 cm(-1) due to their different OH hydrogen-bonding patterns.

257 Hydrogen bonding plays a crucial role in Bronsted acid c

258 d-activated endosomal escape in living cells.Hydrogen bonding plays a major role in determining the t

259 Hydrogen bonding plays an essential role on intermolecul

260 iple retention mechanisms (e.g., dispersion, hydrogen bonding, polar, and ionic) for solute solubiliz

261 Thus, sidechain hydrogen-bonding potential is satisfied in a manner that

262 nation of van der Waals packing and Calpha-H hydrogen bonding predicts the experimental trend of dime

263 The different hydrogen bonding properties in OSM and dihydro-OSM bilay

264 SM with comparable dihydro-SMs, because the hydrogen bonding properties of SM and dihydro-SM differ.

265 he thiourea are usually used to increase the hydrogen-bonding properties, such as 3,5-bis(trifluorome

266 uding electrostatics, stability and folding, hydrogen bonding, protonation, solvation, dynamics, and

267 erite reversibly adsborb linear pentenes via hydrogen bonding, rapidly isomerizing the double bond.

268 nding affinity for anions corresponds to the hydrogen-bonding receptor 7(2+).2PF6(-).

269 Apart from Lewis acid-base recognition, hydrogen bonding recognition is also compatible with thi

270 eation, finding that the desolvation/loss of hydrogen bonding required to leave the membrane partitio

271 the significant local unfolding and loss of hydrogen bonding seen in molecular dynamics simulations.

272 sion and greater sensitivity to polarity and hydrogen bonding solvents relative to previously known d

273 es, including nonpolar, aromatic, polar, and hydrogen bonding solvents.

274 red by electron-withdrawing substituents and hydrogen-bonding solvents.

275 ons of Ascona B-DNA consortium, we extracted hydrogen bonding, stacking and solvation energies of all

276 in environment significantly affects the HNO hydrogen bonding structures and properties.

277 The pyridyl-acyl E-hydrazone acts as a hydrogen bonding template that directs the assembly of a

278 teractions associated with molecular motion, hydrogen bonding tendencies, thermally activated soft oc

279 that in addition to direction resulting from hydrogen bonding, the dipole moment of the ion-pair tran

280 assist to adsorb the uranyl sulfates through hydrogen bonding thus facilitated electro-reduction.

281 ntrast, fluoride as a counterion favors dual hydrogen bonding to both hydroxy groups leading to equat

282 lecules with sequence (GAGAGAGQ)10 stack via hydrogen bonding to form fibrils which have been themsel

283 phile, while the nitroalkene coordinates via hydrogen bonding to the ammonium function of the quinucl

284 two key principal amine compounds imposed by hydrogen bonding to water, where a pH-dependent excitati

285 ompetitive epoxidation pathways, promoted by hydrogen-bonding to either the in situ formed ammonium m

286 ion state being coupled with assistance from hydrogen-bonding to the ammonium moiety.

287 um moiety disfavoring conformations in which hydrogen-bonding to the hydroxyl group results in direct

288 onstrate the generality of the Bronsted acid-hydrogen bonding transition state (TS) model for cinchon

289 imethylsiloxanes end-functionalized with the hydrogen-bonding ureidopyrimidinone (UPy) motif undergo

290 ces may be used to replace the complementary hydrogen bonding used by natural pairs and represents a

291 The strength of the hydrogen bonding was estimated as 0.94 and 0.64 kcal/mol

292 DNA structures stabilized by inter-base-pair hydrogen bonding was observed.

293 link HMW-GS via hydrophobic interactions and hydrogen bonding, whereas their interaction with gliadin

294 Dual hydrogen bonding will eventually differentiate between d

295 Hydrophobic interactions are accompanied by hydrogen bonding with beta5i and beta6 subunits.

296 All NESs also participate in main chain hydrogen bonding with human CRM1 Lys568 side chain, whic

297 compounds were designed to yield additional hydrogen bonding with residues of the Cif active site.

298 The hydrogen bonding with the amide groups in the side chain

299 oxylate side chain metal ligand to allow for hydrogen bonding with the substrate, and creation of a t

300 ps for stabilizing key intermediates through hydrogen bonding with water molecules during hydride tra