ライフサイエンスコーパス: hydrogen bond

1 he Z-isomers having bifurcated O-H...O...H-X hydrogen bond.

2 rate, a position indicative of a low-barrier hydrogen bond.

3 l by a transient, Ser mediated, intrahelical hydrogen bond.

4 nt results in a P*U pair containing only one hydrogen bond.

5 ghly corresponds to the breakage of a single hydrogen bond.

6 ride anion by formation of a unique B-FH-O-B hydrogen bond.

7 rophobic packing and by a complex network of hydrogen bonds.

8 ithout the formation of correct Watson-Crick hydrogen bonds.

9 the formation of larger networks of Calpha-H hydrogen bonds.

10 n delocalization and formation of two strong hydrogen bonds.

11 on of geometric and functional properties of hydrogen bonds.

12 matic cores, and an ability to form multiple hydrogen bonds.

13 olved in DNA contacts, including directional hydrogen bonds.

14 its solvent cage and then to the symmetry of hydrogen bonds.

15 a geometry better-suited for intramolecular hydrogen bonding.

16 nucleophile binds to the thiourea moiety by hydrogen bonding.

17 instead with precursor complex formation by hydrogen bonding.

18 roscopy we probe changes in conformation and hydrogen bonding.

19 nitrate, bicarbonate and sulfate anions via hydrogen bonding.

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

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

22 sugar binding in all GLUT1 conformations via hydrogen bonding.

23 ultiple, traditionally stronger oxygen-based hydrogen bond acceptors.

24 The hydrogen bond acidity parameters A (0.085-0.126) were de

25 hich AMP binding triggers a rearrangement of hydrogen bonds across the large and small interfaces.

26 Subsequent reaction with hydrogen-bond activated dialkyl azodicarboxylates delive

27 ns proceed by pre-equilibrium formation of a hydrogen-bonded adduct between TEMPOH and the pyridine b

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

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

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

31 gy function, which led us to re-parameterize hydrogen bond and electrostatic potential energy functio

32 l cyclization step through an intermolecular hydrogen bond and the phosphate anion promotes proton tr

33 e synergy between the phosphoric acid OH...O hydrogen bond and the secondary CH...O formyl hydrogen b

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

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

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

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

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

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

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

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

42 providing residue contacts for a network of hydrogen bonds and a salt bridge in the core of binding.

43 The formation of hydrogen bonds and carboxylate ionic bonds at the interf

44 sting of charged molecules, held together by hydrogen bonds and Coulomb interactions, have attracted

45 tion of gels, with variations related to the hydrogen bonds and hydrophobic interactions, which occur

46 Intersubunit interactions involving 11 hydrogen bonds and numerous hydrophobic contacts account

47 ations strengthen networks of water-mediated hydrogen bonds and reduce binding affinity by increasing

48 nd intermolecular interactions stabilized by hydrogen bonds and salt bridges can hinder the separatio

49 hydrophobic, and halogen bond contacts, and hydrogen bonds and specific atom-aromatic ring (cation-p

50 Indeed, they share hydrogen bonds and Van der Waals and electrostatic inter

51 amide sp(2)N interactions (proposed n-sigma* hydrogen bond) and amide sp(2)O-aromatic sp(2)C (propose

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

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

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

55 : GmhA instead employs a delicate network of hydrogen bonds, and couples pairs of active sites contro

56 describes the balance among covalent bonds, hydrogen bonds, and van der Waals interactions that dict

57 ving intramolecular O-H...O horizontal lineC hydrogen bond are converted by UV irradiation to the Z-i

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

59 We find that weak hydrogen bonds are at or near preferred gamma-secretase

60 h severe NMR line broadening until the final hydrogen bonds are formed.

61 Especially hydrogen bonds are known to have special geometric requi

62 the hypothesis that the networks of Calpha-H hydrogen bonds are major contributors to the free energy

63 argely because reversible crosslinks such as hydrogen bonds are often polar motifs, whereas covalent

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

65 ydrogen bond and the secondary CH...O formyl hydrogen bond as the reaction occurs.

66 ollowed by ring-closing, but support instead hydrogen-bond assisted ring-closing to prodrugs.

67 Hydrogen bonding at the indole amine most likely stabili

68 es of SPs based on the 1D exotic stacking of hydrogen-bonded azobenzene hexamers.

69 The hydrogen-bond-based resorcinarene capsule represents the

70 Finally, we show that a single hydrogen bond between a glutamic acid (E90) and an aspar

71 atures which facilitate catalysis, such as a hydrogen bond between a main chain nitrogen atom and the

72 of an equal amount of N-Cl-DCAM by forming a hydrogen bond between hypochlorite oxygen and amino hydr

73 Although the crystal structure shows a hydrogen bond between the iron bound aspartate and the b

74 om partial charge analysis, we find that the hydrogen bond between the Thr196 residue of SpnF and the

75 tal structure, including the importance of a hydrogen bond between Thr-238 and the substrate as well

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

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

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

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

80 98 K and 1 bar (6.0 mmol g(-1)) and involves hydrogen bonding between the OH group of the host and th

81 ACE inhibition relies on the formation of hydrogen bonds between C-terminal residues of lentil pep

82 loops are polydisperse and bind via a set of hydrogen bonds between disordered side chains.

83 Below 10% MC, water molecules tend to break hydrogen bonds between polymer chains and form new hydro

84 he Q177K mutation results in a disruption of hydrogen bonds between Q177 and the ligand-binding resid

85 ith E353, which is critical for inducing key hydrogen bonds between talin2 N326 and beta1-integrin R7

86 This interfacial location is stabilized by hydrogen bonds between the 5-HT hydroxyl group and lipid

87 to ABA receptors by increasing the number of hydrogen bonds between the compound and the surrounding

88 from the membrane is lowered by a network of hydrogen bonds between the lipid molecule and PITPalpha;

89 h the CA II active site zinc, as well as two hydrogen bonds between the oxazolidinedione ring oxygen

90 The FTIR analysis indicated the formation of hydrogen bonds between the polar zone of phospholipid an

91 162 and glutamic acid 173, form stabilizing hydrogen bonds between the PsbS monomers only at high lu

92 is stabilized by Arg54 and Glu76, which form hydrogen bonds between two subunits.

93 en bonds between polymer chains and form new hydrogen bond bridges between the polymer chains, while

94 ree volume reduction along with formation of hydrogen bond bridges causes a growth in elastic modulus

95 alt bridges) and dipole-dipole interactions (hydrogen bonds), but nevertheless represents a distincti

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

97 The directed activation of carbon-hydrogen bonds (C-H) is important in the development of

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

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

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

101 ts are descriptors of the molecular size and hydrogen bond capacity.

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

103 1,3-Disiloxanediols are effective hydrogen-bonding catalysts that exhibit enhanced activit

104 ated with the existence of an intramolecular hydrogen bond (CH...N) between the six-membered ethene b

105 monas reinhardtii (Cr) ChR2) (i) undergoes a hydrogen bond change in D --> K transition and (ii) depr

106 igated so far, proton transfer reactions and hydrogen bond changes are crucial for the formation of t

107 s results in the irreversible formation of a hydrogen-bonded complex between the singlet carbene and

108 y, the particle formation from the gas-phase hydrogen-bonded complexes of HMSA with (R1)(R2)NH on the

109 e receptor well and were predicted to form a hydrogen-bond conserved among known agonists.

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

111 electrostatic interactions, pi-pi stacking, hydrogen bonds, coordination bonds, and dynamic covalent

112 form ammonia monohydrate from a prototypical hydrogen-bonded crystal into a form where the standard m

113 value is compared to the thermodynamics of a hydrogen bond determined by similar methods.

114 ions within a scaffold organized by multiple hydrogen bonds dictate stereoselectivity.

115 The tetramers consist of hydrogen-bonded dimers that sandwich together through hy

116 r wall is composed of an extended network of hydrogen-bonded dimers.

117 an unusual elongated main chain nitrogen to hydrogen bond distance positioning the hydrogen atom tow

118 Hydrogen bonds dominate many chemical and biological pro

119 C2-symmetric, dual hydrogen-bond donating bistriflamides are shown to be hi

120 ve catalytic approach through inclusion of a hydrogen bond donor cocatalyst significantly improved en

121 ound that the difluoromethyl group acts as a hydrogen bond donor on a scale similar to that of thioph

122 talysts despite the absence of an additional hydrogen bond donor or acceptor site (i.e., the presence

123 s more preorganized and the higher number of hydrogen bond donor sites provides a remarkable enhancem

124 otency, it simultaneously introduces a third hydrogen bond donor that limits brain availability and p

125 thyl group, as it is considered a lipophilic hydrogen bond donor that may act as a bioisostere of hyd

126 design of a new protocol in which an achiral hydrogen bond donor thiourea catalyst was utilized to en

127 gate for the OH group, can act as an unusual hydrogen bond donor, as confirmed by crystallographic, s

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

129 d number of hydrogen bond sites (less than 4 hydrogen bond donors and 10 acceptors), with a moderate

130 A bifunctional macrocycle, with hydrogen bond donors at one end and acceptors at the oth

131 nctional groups and neutral and cationic C-H hydrogen bond donors, as well as underexplored strong di

132 The conformational and hydrogen-bond dynamics of the D-channel residue N139 is

133 tal lineO...H-N and C horizontal lineO...H2O hydrogen bonds, elucidating their role in the brush's te

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

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

136 It was found that an intramolecular hydrogen bond favors an increase of the quantum yield of

137 ion on the microscopic properties of a given hydrogen-bonded fluid.

138 The oxidative addition of element-hydrogen bonds, for example, represents a critical step

139 Hydrogen bond formation has been identified between the

140 Hydrogen bonds formed between the backbone of His55 and

141 attributed to fluctuations of the number of hydrogen bonds formed between water and the three carbon

142 near arrangement coexists with three regular hydrogen bonds formed by lysine NH3(+) group (angle C(ep

143 l compartments of a crystalline zeolite-like hydrogen-bonded framework illustrates a unique approach

144 1,3 fashion to the fully reduced state, with hydrogen bonding from Lys397, and two electrons are tran

145 Hydrogen-bonding from MeOH is critical for the hyponitri

146 MR may help in discriminating among free and hydrogen-bonded functional groups.

147 Inspired by the hydrogen-bonded G-quadruplexes found frequently in guani

148 ing approaches a more general description of hydrogen bond geometries, using distance and directional

149 Detailed information on the hydrogen bond geometry upon hydrogen-to-deuterium isotop

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

151 ongstanding controversy on the nature of the hydrogen bond (HB) can be settled by looking at the effe

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

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

154 Inspired by the concept of hydrogen bond, herein we focus on the Li bond chemistry

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

156 forces including electrostatic interactions, hydrogen bonds, hydrophobic interactions, and van der Wa

157 Intramolecular hydrogen bonds (IMHBs) in 5-azopyrimidines are investiga

158 The strength of the formyl hydrogen bond in the TS, a second CH...O interaction bet

159 1 degrees C gives insight into the extent of hydrogen bonding in supercritical water.

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

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

162 e the electrostatic screening (shielding) of hydrogen bonds in bulk water as the critical element for

163 or for accurately determining intermolecular hydrogen bonds in carbohydrate-protein complexes.

164 ectroscopy (FTIR) proposed formation of more hydrogen bonds in gel due to NLC loading or citric acid-

165 groups and the important roles of CF2-H...O hydrogen bonds in influencing intermolecular interaction

166 The preponderance of hydrogen bonds in intermolecular associations amongst mo

167 hydrogen atom abstraction from the nitrogen-hydrogen bonds in purine nucleosides produces reactive i

168 th several specific hydrophobic contacts and hydrogen bonds in the cap domain.

169 of the molecule on top by strengthening the hydrogen bonds in the layer that it contacts.

170 Although backbone hydrogen bonds in transmembrane (TM) helices have the po

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

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

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

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

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

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

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

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

179 nformation, whereas its substitution affects hydrogen bond interactions at position 70, required for

180 factor-bound aminoacyl-tRNA is initiated by hydrogen bond interactions between the first two nucleot

181 ocking transition state and tertiary A-minor hydrogen bond interactions form after the docking transi

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

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

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

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

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

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

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

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

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

191 r results highlight the role of stacking and hydrogen-bond interactions in restraining amino-group ro

192 6 interact with acidic residues that mediate hydrogen-bond interactions with the ubiquitin Lys48 side

193 ater-FeS(001) interface through a network of hydrogen-bonded interactions with water molecules on the

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

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

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

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

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

199 unique bioinspired environment with multiple hydrogen-bonding interactions.

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

201 he Crwn-THF moiety of GRL-09510 forms strong hydrogen-bond-interactions with HIV-1 protease (PR) acti

202 elf-assembly of multiple building blocks via hydrogen bonds into well-defined nanoconstructs with sel

203 n order to determine the contribution of the hydrogen bond involving the exocyclic amino group.

204 This hydrogen bond is characterized by a short H-F distance o

205 nd structural characteristics of low-barrier hydrogen bond (LBHB) formation are well documented in th

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

207 icative of the presence of noncovalent C-Hpi hydrogen-bond-like interactions involving the amide pi n

208 e a wide range of residues, while main chain hydrogen bonds may help dictate substrate-binding orient

209 protocol was essential to guarantee that the hydrogen bond-mediated signalling mechanism between the

210 e proximity of the pyridinyl nitrogen to the hydrogen bond microenvironment.

211 drastically rearranges a network of proximal hydrogen bonds, modifying the local architecture of a wa

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

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

214 We demonstrate that this hydrogen bond network directly influences the protonatio

215 The hydrogen bond network includes a strictly conserved Tyr

216 A complex hydrogen bond network of four active site residues, whic

217 signaling modules through rearrangement of a hydrogen bond network previously identified in the CD247

218 analysis demonstrates a modification in the hydrogen bond network related to residue 24, while Norma

219 the progressive breaking of the tetrahedral hydrogen bond network that makes water so peculiar.

220 FAD (BLUF) photoreceptors is surrounded by a hydrogen bond network that senses and responds to change

221 ibutes crucially to ligand sensitivity via a hydrogen bond network, where Arg interacts both with ago

222 picting the time-dependent disruption of the hydrogen bond network.

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

224 ere is a significant population shift in the hydrogen-bonded network and salt bridges involving side

225 ons in positions, or communication along the hydrogen-bonded network depends on the protonation state

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

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

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

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

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

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

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

233 elatively humidity, attributed to the formed hydrogen-bond networks between the DNA molecules and the

234 se compounds crystallize to form robust open hydrogen-bonded networks with parallel indenofluorenyl c

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

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

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

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

239 ser degree of interaction, leading to normal hydrogen bonds of type YH-X analogous to secondary bondi

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

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

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

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

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

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

246 00 and 3700 cm(-1) due to their different OH hydrogen-bonding patterns.

247 e computational ability to switch on and off hydrogen bonds permitted us to identify which, among the

248 adsorbed pentene in ZSM-5 and the localized hydrogen-bonded pi-complex at Bronsted acid sites, -36 k

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

250 ls were used to directly quantify DMSO/water hydrogen-bond populations in binary mixtures.

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

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

253 he metal carbonyl headgroup shows that water hydrogen bond rearrangement dynamics slow from 1.5 ps in

254 e interactions, hydrophobic interactions and hydrogen bonds, respectively, lowering significantly the

255 Through-hydrogen-bond scalar coupling is investigated in (15)N l

256 ocks out a Watson-Crick-type (G)N2H2...O2(T) hydrogen bond, significantly destabilized the transient

257 affold functionalized by a limited number of hydrogen bond sites (less than 4 hydrogen bond donors an

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

259 tide backbone's carbonyl and amide groups in hydrogen-bond stabilization of helical structures is a m

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

261 Hydrogen bonds suggested by atom-atom distances from neu

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

263 re numerous, and more tetrahedrally oriented hydrogen bonds than those in bulk water and that their m

264 of fluorines that can undergo intramolecular hydrogen bonds that form 5-8-membered cycles with modera

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

266 rface; the cationic headgroups form multiple hydrogen bonds, thus crosslinking TLRs into functional c

267 Herein, we show that an intramolecular hydrogen bond to the aqua ligand can reduce this interna

268 flexibility, steric factors, and ability to hydrogen bond to the polymerase modulates rapid and accu

269 emarkable ability of a strategically located hydrogen bond to transcend the normal regioselectivity o

270 eral arrangement of adsorbed water molecules hydrogen bonded to terminal aquo groups.

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

272 gned to self-assemble through intermolecular hydrogen bonds to beta-sheets thereby placing the azide

273 A tyrosine that hydrogen bonds to propionate 2 in a position analogous t

274 of triazolium groups that act together to CH-hydrogen-bond to halide anions when the macrocycle is lo

275 histidine and conclude that the histidine is hydrogen-bonded to N2, tuning its reduction potential.

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

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

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

279 poxidation reaction by the potential to form hydrogen-bonds to two directing groups rather than one i

280 polypeptide backbone forms transient, sparse hydrogen-bonded turns and remains significantly hydrated

281 horizontal lineC component of the bifurcated hydrogen bond upon the formation of the C horizontal lin

282 he formation of the C horizontal lineO...H-X hydrogen bond was found experimentally, proved theoretic

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

284 o-hydrogen of the phenyl ring and the OH...O hydrogen bond were determined using quantum mechanical c

285 sible modes of dual activation mechanism via hydrogen bonds were considered.

286 nding is assisted by the formation of a C-HF hydrogen bond which involves a methine group of the 1,8-

287 last guanine nucleotides form water-mediated hydrogen bonds, which aid in ligand recognition.

288 PC results in the formation of protein-lipid hydrogen bonds, which alter the dynamics of the ester gr

289 ed this interaction to be a weak to moderate hydrogen bond with a C-H stretch vibration frequency blu

290 ese results suggest that talin2 S339 forms a hydrogen bond with E353 to mediate its high affinity to

291 ing analysis shows that talin2 S339 formed a hydrogen bond with E353, which is critical for inducing

292 ively "deep" in the CaM-BD/CaM interface and hydrogen bond with E54 on CaM.

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

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

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

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

297 ach conserved nucleotide makes base-specific hydrogen bonds with a particular residue.

298 rast, NS309 sits more "forward" and directly hydrogen bonds with R362 in KCa3.1.

299 d 300 degrees C biochar likely formed strong hydrogen bonds with the citrate layer of nAu.

300 ructure, solvent accessibility and sidechain hydrogen bonds, XSuLT annotates each amino acid residue