ライフサイエンスコーパス: psi

1 ens offset (-5 V), auxiliary gas pressure (0 psi), and isolation width of parent ion (m/z value = 3).

2 nder optimized processing conditions (10,000 psi and 2 passes).

3 As expected, digestion efficiency at 10,000 psi was increased and reproducibly produced more peptic

4 rolonged, continuous high-pressure at 10,000 psi.

5 iquid chromatography at approximately 11,000 psi on sub 2-microm particles combined with reversed-pha

6 essures up to approximately 1000 bar (15,000 psi).

7 ed by high pressure homogenization at 25,000 psi.

8 c pressure to 2000 bar (approximately 30,000 psi) at 25 degrees C.

9 ed at a pressure as high as 2070 bar (30,000 psi).

10 ment compared with hydrodynamic injection (1 psi, 10 s).

11 (i)) and the psi angle of the residue i - 1 (psi(i-1)) on the 0.1 ps time scale.

12 d S8 under near-ambient conditions (e.g., 10 psi, 25 degrees C).

13 nflammation were observed in pressures >= 10 psi and orientation effects were observed at pressures >

14 system that operates at low pressures (< 10 psi).

15 At low pressures (<10 psi), elevated indicator bacteria were frequently detect

16 gh pressure [>20 psi], low pressure [5 to 10 psi], or very low pressure [1 to 2 psi]) and one of two

17 bient pressure could withstand more than 100 psi without failure.

18 re unchanged even to 120 degrees C under 100 psi of O2 and in the presence of active radical chains (

19 ucted by reacting 2(TFE)-(13)C with 300-1000 psi of methane in single-crystal sapphire NMR tubes; cle

20 (CH3CN)2 from voltammograms recorded at 1000 psi of H2.

21 ore peptic peptides versus digestion at 1000 psi.

22 From 40 to 120 psi, both regioisomer (b:l) and enantiomer (R:S) ratios

23 ion effects were observed at pressures >= 13 psi.

24 3 Sprague Dawley adult rats to unilateral 14 psi blast exposure to induce tinnitus and measured audit

25 ontrolled apparatus at 40 degrees C and 1400 psi (9.65 MPa).

26 ross fitting and can withstand at least 1400 psi.

27 s of 4a under H(2) and D(2) atmospheres (150 psi), which leads to the exclusive formation of the bis(

28 , a pressure drop of only approximately 1500 psi is sufficient to maintain an effluent flow rate of <

29 troller and could hold up to 1100 bar (16000 psi) of pressure.

30 At pressures between 10 and 17 psi, evidence of periodic contamination suggested that t

31 ith a chlorine residual and at pressures >17 psi.

32 Using a 2 min injection with 18 psi counter-pressure, 50% of the cells injected into the

33 nd laterally at a pressure range of ~ 8.5-19 psi, for up to 30 daily exposures.

34 [5 to 10 psi], or very low pressure [1 to 2 psi]) and one of two irrigation solutions (castile soap

35 ll 400 mum holes in carbon steel pipes at 20 psi self-repaired at pH 4.0-11.0.

36 Similar leaks in carbon steel pipes at 20 psi self-repaired at pH 5.5 and 8.5, but two leaks did n

37 retically or by pressure pulses (10 ms at 20 psi) into the taste-responsive regions of the NST and th

38 ree irrigation pressures (high pressure [>20 psi], low pressure [5 to 10 psi], or very low pressure [

39 a and thereafter decreases abruptly by 1,200 psi (8.3 MPa) over 370 ft (113 m) as the main sandstone

40 iquid-liquid separations run at or above 200 psi to provide solvent-free product, and the use of high

41 m tetraborate solution eluent (typically 200 psi) as the pump, and performing on-column detection usi

42 l pressures above 20 MPa (approximately 2900 psi) for efficient pressure-driven HPLC separations.

43 INDUCIBLE 1A (RCI1A) gene encodes the 14-3-3 psi isoform.

44 x between an RNA hairpin derived from the 3' psi pocket of human U65 H/ACA small nucleolar RNA (snoRN

45 dized with 0.5 mol % Pd/Au (3:1)-17 under 30 psi of oxygen in water to give the dihydroxylated produc

46 Rats received two 30-psi (~ 207-kPa) blasts 24 h apart or were handled identi

47 els was observed at pressures as high as 300 psi.

48 hannel, capable of withstanding at least 300 psi, is demonstrated.

49 in 78% yield under catalytic conditions (35 psi H(2)), presumably by the 5-exo-trig cyclization of t

50 ed that some of the repairs created at 20-40 psi ambient pressure could withstand more than 100 psi w

51 formation of corrosion precipitates at 20-40 psi, pH 3.0-11.0, and with upward and downward leak orie

52 er exchange under low-pressure operation (40 psi), parameters such as the size exclusion resin, load

53 PEM under the same operating conditions (400 psi, 50 degrees C).

54 withstand pressures up to approximately 4000 psi.

55 egrees C, 10s of hydrodynamic injection (0.5 psi) and UV detection at 254 nm.

56 osed to blast wave pressure of 300 kPa (43.5 psi) per day for 3 successive days, and euthanized 30 da

57 Experimental data demonstrated ~ 8.5 psi is the threshold for hemorrhage/contusion, up to 30

58 as flow of 6 mL/min, nebulizer pressure of 5 psi, and drying gas temperature set to 200 degrees C.

59 s under mild conditions (35 degrees C and 50 psi CO/H(2)), and Z-olefins afford excellent enantiosele

60 ely low-pressure catalytic hydrogenation (50 psi of hydrogen) was employed using Raney nickel as the

61 nd with increasing TMP up to a maximum of 50 psi (3.45 bar).

62 ylene pressure was increased from 100 to 500 psi in order to produce semicrystalline ethylene-rich en

63 onic Rh(I)-Josiphos complex in THF under 500 psi of H2 generated the corresponding tertiary carbinami

64 50 exposures with intensity thresholds at 8 psi for front exposure and 6psi for side exposures, whic

65 uthenium dodecacarbonyl catalyst under 40-80 psi of CO.

66 endent of CO pressure up to 80 psi; above 80 psi one observes the onset of inhibition.

67 and N(2) pressure found to be 3206 V and 80 psi, respectively.

68 ted alkynes were acceptable substrates at 80 psi of ethylene.

69 is of CRP, including sheath gas pressure (80 psi), capillary temperature (275 degrees C), collision e

70 ation is independent of CO pressure up to 80 psi; above 80 psi one observes the onset of inhibition.

71 9 lbs) and could generate up to 55 MPa (8000 psi) pressure.

72 e solvent was changed and pressurized to 900 psi.

73 A psi equal to zero or one indicates that the biHis site i

74 ed macrocycles and classify them according , psi, and omega torsion angles.

75 In contrast, the deltaPKC activator, psi deltaRACK, injected at reperfusion, reduced ERK1/2 p

76 nd the specific PKC epsilon peptide agonist, psi epsilonRACK, each activated mitoK(ATP)-dependent K+

77 priming by the selective PKCepsilon agonist, psi epsilon receptor for activated c kinase (psiepsilonR

78 te U-C(4) pai-bonds utilising the psi(2) and psi(3) molecular orbitals of the C(4) -unit, but the pot

79 revealed almost all known m(5)C, m(1)A, and psi sites in tRNAs and rRNAs and provided hundreds of ne

80 ational models of linkage torsion angles and psi in solution, which were compared to those obtained f

81 ons of protein backbone torsion angles ( and psi) and secondary structure from sequence are crucial s

82 ags (x, y, z: space; t: time of arrival; and psi: angle of linear polarization) at 100 billion frames

83 mp loading reaction by two subunits, chi and psi, which are not present in the crystal structures, we

84 TASS, the mean absolute errors for final and psi predictions are further decreased to 16.28 and 21.98

85 , OPUS-TASS achieves 16.56 and 22.56 for and psi predictions, and 89.06 and 78.87% for 3- and 8-state

86 n absolute errors of 16.89 and 23.02 for and psi predictions, respectively, and the accuracies for 3-

87 y in cap methylation, 3'-end maturation, and psi(28) formation.

88 eractions of nucleocapsid protein (NCp7) and psi-RNA.

89 orporation of the experimental models of and psi into the backbone of an octasaccharide fragment lead

90 he evolutionary correlations between P50 and psi(min) and between K(s) and Hv show signs of deeper ev

91 e native structure by changing every phi and psi angle by either +/-3, +/-5 or +/-7 degrees, five sma

92 lear preference for adopting helical phi and psi angles in the pH 2.0 unfolded state.

93 ep learning architectures to predict phi and psi angles of protein backbone.

94 The mean absolute error (MAE) of phi and psi angles predicted by DRNN, DReRBM, DRBM and DNN is ab

95 imilarity metrics such as changes in phi and psi angles.

96 trong preference to populate helical phi and psi angles.

97 n of the RNA backbone, comparable to phi and psi in the protein backbone.

98 4 to preferentially populate helical phi and psi values in the unfolded state.

99 mine the Ramachandran torsion angles phi and psi.

100 xes revealed similar ranges of phi (phi) and psi (psi) angles between iduronate and glucosamine rings

101 membrane if and only if Gag was present and psi was intact.

102 pically in mini c TAR DNA, mini TAR RNA, and psi(3) RNA, but at 5 degrees C, the motion became more a

103 rmation in much the same way that varphi and psi are used to describe backbone configuration of prote

104 ibility in the backbone dihedrals varphi and psi as well.

105 dependent constraints on backbone varphi and psi torsion angles in samples with sequential pairs of c

106 echanical bonds (corresponding to varphi and psi) that include realistic barriers to rotation that cl

107 n of the backbone dihedral angles varphi and psi.

108 lowing for control of the omega, varphi, and psi dihedral angles adopted by the systems.

109 ifts are dominated by local torsion angles , psi, chi1; hence, these experiments identify flexible to

110 The vRNA packaging signal, known as psi, inhibited imp-alpha binding to Gag, indicating that

111 The first band (psi) is centered between 260-280 Hz; the second, and str

112 that vRNA is selected for packaging because psi nucleates assembly more efficiently than other RNAs.

113 the ATPase spiral observed upon DNA binding, psi binding promotes the clamp-loading activity of the c

114 oach and identified 4187 proteins from both [psi (-)] and [PSI (+)] strains.

115 traditional stress vs. life (S-N) curves by psi, where psi is the proportion of material oriented tr

116 r mimic of stem-loop 3 RNA (SL3, also called psi-RNA, in the packaging domain of genomic RNA) is stro

117 The DnaX complex (DnaX(3)deltadelta'chi psi) within the Escherichia coli DNA polymerase III holo

118 two NC-binders to inhibit viruses containing psi-region deletions (DeltaSL1 or DeltaSL3) and found th

119 landscape of psi over which stomata control psi, and (2) the slope of the daily range of psi as pre-

120 e novo induced cultures are able to convert [psi (-)] cells to [PSI (+)] cells.

121 bsence of competition with the corresponding psi transcripts lacking SL1 or SL3 for binding DP6-Gag i

122 sslink-values agree with their corresponding psi-values when they have both have values of zero or on

123 -values are smaller than their corresponding psi-values, the apparent underestimation of structure fo

124 ution of unfolding forces for the protein D, psi(D)(f).

125 slope of the daily range of psi as pre-dawn psi declined, were strongly correlated with each other a

126 hat before autophagy mitochondria lose delta psi(m) and OPA1, and that overexpression of OPA1 decreas

127 -2 antagonist, rapidly induced loss of Delta psi m and caspase-9 activation but had no effect on the

128 mitochondrial transmembrane potential (Delta psi m) and weak caspase-9 activation, whereas thapsigarg

129 the mitochondrial membrane potential (delta psi m).

130 xhibited increased membrane potential (delta psi(m)) and a high probability of subsequent fusion, whi

131 ondria that were found to have reduced delta psi(m) and decreased levels of the fusion protein OPA1.

132 der, gamma(3)deltadelta', gamma(3)deltadelta'psi, and gamma(3)deltadelta'psichi.

133 s of residues with experimentally determined psi of unity.

134 tant progress on the 3D structure of dimeric psi.

135 od of estimation of the parent distribution, psi(D)(f), based on analyzing the force data for a tande

136 uctural similarity with the so-called double-psi barrel family of proteins.

137 -MS) to measure the 15N relative exceedance, psi(15N), of HONO in the gas-phase.

138 ce constraints derived from the experimental psi-values.

139 tive to leaf area (Hv) and drought exposure (psi(min) ), and matched it with global seed plant phylog

140 t our results in a simple correction factor, psi, the ratio of the corrected Young's modulus and the

141 (26.1 copies per 10(6) cells), negative for psi and integrase, and negative by the intact proviral D

142 A role for psi in stabilizing or promoting ATP- and ATPgammaS-induc

143 ative-like, respectively, while a fractional psi implies that in the TSE, the biHis site recovers onl

144 When a site with a fractional psi lies adjacent to a site with psi = 1, the fractional

145 acent to a site with psi = 1, the fractional psi generally signifies that the "fractional site" has a

146 counted for by the proportion of prion-free [psi(-) ] cells present, no change in the molecular weigh

147 cell division thereby generating prion-free [psi(-) ] cells.

148 stronger strain of [PSI+] and convert from [psi-] to [PSI+] with a much higher frequency.

149 ntaining the isostere, Ac-(Gly-Pro-Hyp)3-Gly-psi[(E)CH C]-Pro-Hyp-(Gly-Pro-Hyp)4-Gly-Gly-Tyr-NH2, had

150 When phi crosslink > psi, the apparent inconsistency is rationalized by the d

151 imization (4) predicts systematically higher psi(l) than (1-3), pointing to the need of an updated de

152 Stem-loop 3 RNA (SL3) in psi-RNA is a highly conserved motif in different strains

153 These binding sites are used in psi analysis studies to investigate structure formation

154 oorly with the nonaggregated Sup35 found in [psi(-)] cells.

155 used bioinformatics applications, including (psi)-blast, modeller, muscle and Primer3, and tools are

156 The inability of these aptamers to inhibit psi-deleted viruses correlated with the absence of compe

157 d solute accumulation of ahk1 mutants at low psi(w) suggest that AHK1 may not be the main plant osmos

158 umulation was reduced in ahk1 mutants at low psi(w).

159 Expression of AHK1 itself was reduced by low psi(w), in contrast to previous reports.

160 s had enhanced growth maintenance during low psi(w), while hin1 mutants had reduced growth, further i

161 e the main plant osmosensor required for low psi(w) tolerance.

162 d, solute accumulation across a range of low psi(w) severities.

163 ahk1 mutants had reduced low psi(w) induction of Delta(1)-Pyrroline-5-Carboxylate Syn

164 than 500 introns where moderate severity low psi(w) altered intron retention (IR) frequency.

165 prion, inhibits growth of [PSI(+)] but not [psi(-)] cells.

166 lication, and disruption of the nucleocapsid-psi-RNA complex interferes with viral replication.

167 milarity and fit of predicted and observed [/psi] main chain dihedral angle propensities.

168 mp partially compensates for the activity of psi when this subunit is not present and possibly serves

169 esults demonstrate the unique application of psi-value analysis in elucidating the structure of the t

170 Calculation of psi and phi dihedral angles from the chemical shift assi

171 allenging protein, we apply a combination of psi analysis (which probes the role of specific side-cha

172 metrics of stringency of stomatal control of psi, (1) a 'hydroscape' incorporating the landscape of p

173 =0.2-0.5, the relative standard deviation of psi(15N) is <4%.

174 pment of ligands that target the elements of psi-RNA of HIV-1 with high affinity and specificity.

175 chanistic investigation to another family of psi synthases and an enzyme that makes an adduct with f5

176 'hydroscape' incorporating the landscape of psi over which stomata control psi, and (2) the slope of

177 able to the existing methods, but the MAE of psi angle is 29 degrees , 2 degrees lower than the exist

178 The magnitude of psi depends on the degree to which an inserted bihistidi

179 ide building blocks, whereas MA'AT models of psi differ.

180 observed between the MA'AT and MD models of psi with respect to mean values and circular standard de

181 psi, and (2) the slope of the daily range of psi as pre-dawn psi declined, were strongly correlated w

182 In the optimal working range of psi(15N)=0.2-0.5, the relative standard deviation of psi

183 rics of stringency of stomatal regulation of psi during soil drying in eight woody species and determ

184 s in src SH3, are compared to the results of psi-analysis where strand association is stabilized by m

185 It generates statistical distributions of -psi dihedral angles based on CS or vice versa.

186 on occurs, providing a further constraint on psi(l) .

187 with Gag in late endosomal foci, again, only psi dependently.

188 Using our psi analysis method along with mutational varphi analysi

189 ccurring alternative p53 splice variant, p53-psi.

190 stribution when the overdispersion parameter psi is 0.

191 alpha) atoms (residues 5-28) is 0.3 A; (phi, psi) angles of D-Ala20 are the same as those of G20 in t

192 amino acids by comparing their backbone phi, psi distributions in different types of secondary struct

193 es continuous estimates of the backbone phi, psi distributions.

194 e orientation but also to its backbone (phi, psi) angles.

195 isotropic chemical shifts and backbone (phi, psi) torsion angles indicate that both TPF4 and TPA4 ado

196 the TM domain, which yielded backbone (phi, psi) torsion angles.

197 of the activation segment, measured by phi, psi, chi1, and pseudo-dihedral angles more accurately cl

198 anizes the collagen peptide main-chain (phi, psi) dihedrals for triple helical assembly.

199 ,916 conformations as a function of the phi, psi, omega, chi1 and chi2 torsional angles for all 20 na

200 istributions around the average values (phi, psi) approximately (-57 degrees , -31 degrees) with a wi

201 ure of KL 4 when bound to lipids, with (phi, psi) angles that differ substantially from common values

202 There are no obvious correlations with phi, psi, chi 1, or chi2 torsion angles, unlike the results s

203 on conformations adopted by two adjacent phi,psi pairs (i.e., (phi,psi)(2) motifs).

204 h we call the niche, with characteristic phi,psi angles, is by far the commonest feature with this pr

205 y an initial exploration of the complex (phi,psi)(2) landscape of proteins, it shows that there is va

206 anosyloxy)-3',4'-didehydro-1',2'-dihydro-phi,psi-caroten -2'-ol, is novel and has been given the triv

207 ed by two adjacent phi,psi pairs (i.e., (phi,psi)(2) motifs).

208 to yield a parameter-dependent list of (phi,psi)(2) motifs, in order of their prominence.

209 resolution or better to create a purely phi,psi-based comprehensive empirical categorization of comm

210 nally rapid algorithm using only single (phi,psi) dihedral angle moves also generates tertiary struct

211 ted level of precision in describing the phi,psi angles of both previously known and novel motifs, or

212 more in-depth characterizations at the (phi,psi)(2) level and at higher dimensions.

213 four-dimensional space based on the two phi,psi pairs to yield a parameter-dependent list of (phi,ps

214 dow ranges in size from a length of 1-10 phi-psi pairs (3-12 residues).

215 Reasonable models have higher-order phi-psi score fit values (m) > -1.00.

216 orithm is based in the geometry and the (Phi-psi)-space conformation of these regions.

217 phi/psi angles alternate in sign along the backbone, as is c

218 bond energy or length/angle and backbone phi/psi angles.

219 ithms for chemical fragments, 3D motifs, phi/psi sequences, super-secondary structure motifs and for

220 This involves a transition of the phi/psi angles of Gly-13 from the right to left alpha-helica

221 al averaging, with essentially uncoupled phi/psi torsion angles.

222 approximately -60 degrees) and more positive psi (> or = 160 degrees) give spectra showing the P(II)

223 pse of the mitochondrial membrane potential (psi(m)).

224 to controlled moderate low water potential (psi(w)) or to salt stress.

225 e-localized HIN1 during low water potential (psi(w)) stress suggested a pre-mRNA splicing-related fun

226 tomatal regulation of plant water potential (psi).

227 pling is controlled by leaf water potential, psi(l) , and determined under four different maximizatio

228 uence similarity to enzymes known to produce psi-end group modifications of carotenoids in proteobact

229 osed TCV hairpins H4a and H4b and pseudoknot psi(3), which are required for the TCV-specific requirem

230 allyl adenine (i(6)A(37)) and pseudouridine (psi(39)).

231 t position 34 (mcm5s2U34) and pseudouridine (psi) at position 39--two of which, ms2t6A37 and mcm5s2U3

232 he first four nucleotides and pseudouridine (psi) formation at uracil 28.

233 ses) isomerize uridine (U) to pseudouridine (psi) in RNA, and they fall into five families that share

234 RNA contains at least one pseudouridylation (psi) pocket, which is complementary to the sequences fla

235 evealed similar ranges of phi (phi) and psi (psi) angles between iduronate and glucosamine rings.

236 The packaging signal psi, at the 5' end of the viral gRNA, binds to Gag throu

237 tiplex ddPCR targeting the packaging signal (psi) and envelope (env).

238 genomic RNA with an intact packaging signal (psi) and Gag were observed to extend outward from the cy

239 cifically compete with the packaging signal (psi) of HIV-1 for binding to DP6-Gag.

240 The packaging signal (psi) of human immunodeficiency virus type 2 (HIV-2) is p

241 al RNA (vRNA) contains a 'packaging signal' (psi) and is packaged as a dimer, with two vRNA monomers

242 e CRISPR loci (termed prokaryotic silencing (psi)RNAs) and the RAMP module (or Cmr) Cas proteins.

243 cleoprotein (snoRNP) particle that guides SL psi(28) formation.

244 amino ester trifluoromethyl aldimines, small psi[CH(CF3)NH]-peptidomimetic backbones can be achieved

245 diastereoselective formation of the 3-spiro-psi-indoxyl moiety in Brevianamide A.

246 ng a dioxopiperazine core and a rare 3-spiro-psi-indoxyl skeleton.

247 on for the dominant-negative effects of such psi-no-more (PNM) mutations and demonstrate directly the

248 Such -psi distributions are used to calculate structural ensem

249 The pseuoduridine synthases (psi synthases) isomerize uridine (U) to pseudouridine (p

250 se III holoenzyme depends upon a Pol III-tau-psi-chi-SSB binding network, where SSB is bound to the d

251 Variation in the terminal psi angles of the NPNA beta-turns results in different d

252 For successful delivery of siKRAS, tGC/psi-nanoparticle formulation of polymerized siRNA and th

253 The psi factor depends on two dimensionless parameters, R/h

254 The psi subunit also increases the affinity of the clamp loa

255 The psi subunit is important for stabilizing an ATP-induced

256 The psi synthase TruA forms a covalent adduct with such RNA,

257 hi angle of the ith residue (phi(i)) and the psi angle of the residue i - 1 (psi(i-1)) on the 0.1 ps

258 ential interaction between HIV-1 Gag and the psi-region that may be distinct from that which occurs d

259 A related structure reveals how the psi protein, essential for coupling the clamp loader to

260 hain stereochemistry, and flexibility in the psi dihedral angle.

261 e genes encoding two enzymes that modify the psi end of myxoxanthophyll in Synechococcus sp. strain P

262 sequence (pal) located at the 3' end of the psi encapsidation signal is critical for human immunodef

263 -OH rather than on the 1'-OH position of the psi end of the molecule.

264 y, cytochrome c release, and collapse of the psi(m).

265 The simulations indicate that the psi = 1 sites by themselves can be used to generate a we

266 rticle, we show structural evidence that the psi pocket can form the predicted base pairs with substr

267 ts from our work and others suggest that the psi subunit may introduce a temporal order to the clamp

268 unit, but the potential delta-bond using the psi(4) orbital is vacant.

269 si-degenerate U-C(4) pai-bonds utilising the psi(2) and psi(3) molecular orbitals of the C(4) -unit,

270 tial energy profile generated by varying the psi dihedral angle in Ace-Pro-NMe indicates that the con

271 The mechanism by which the psi synthases operate remains unknown, and mechanistic w

272 mulation the cells were transformed with the psi AE1A virus.

273 agonist (DAMGO) and deltaOR antagonist (Tipp(psi)), and this leads to a shift in the pattern of ERK1/

274 capsid domain of Gag preferentially binds to psi and Rev Response elements in the viral genome, and G

275 This method is adapted from the traditional psi-value analysis, which uses engineered bi-His metal c

276 a mixed beta-sheet encompassing an uncommon psi-loop motif.

277 l phosphatase (ctAcP) is characterized using psi-analysis, which identifies specific chain-chain cont

278 However, we demonstrate here using psi analysis with engineered metal ion binding sites tha

279 ribution of backbone dihedral angles (varphi,psi) obtained from an experimentally validated denatured

280 freedom per residue, described by its varphi,psi-angles.

281 minates another substantial region of varphi,psi-space for a blocked peptide; for conformers within t

282 steric clashes alone eliminate 3/4 of varphi,psi-space, a result that has guided all subsequent work.

283 To account for the systematic varphi,psi-dependent component of nonplanarity, we present a co

284 Analyses as a function of the varphi,psi-backbone dihedral angles show that the expected valu

285 Comparison with (varphi,psi) distributions from the Protein Data Bank further ju

286 formation, reproduced the 180 degrees varphi-psi dihedral rotation back to the open loop state.

287 ded proteins arising due to intrinsic varphi-psi dihedral angle fluctuations dictate the course of pr

288 he backbone torsional mobility in the varphi-psi dihedral angle space, we used a model intrinsically

289 -range conformational exchange in the varphi-psi dihedral space.

290 tropy in folded proteins by using the varphi-psi distributions of the 20 amino acids in common second

291 h are all down (Cgamma-endo), and the varphi/psi dihedral angles of the Xaa 3(S)Hyp residues are also

292 l stress vs. life (S-N) curves by psi, where psi is the proportion of material oriented transverse to

293 on of U0126 delivered at ischemia onset with psi deltaRACK injected at reperfusion increased infarct

294 fractional psi lies adjacent to a site with psi = 1, the fractional psi generally signifies that the

295 fractional site is distal to the sites with psi = 1, however, the histidines sample configurations i

296 virus particle, interacts specifically with psi, but this is obscured under physiological conditions

297 interaction of the 3' end of the pal within psi with a motif located downstream of SL1.

298 -Gly dipeptide surrogates in the form of Xaa-psi[triazole]-F2Gly building blocks were established, an

299 cent to the accessory sequences from the Xer/psi multimer resolution system, we have imposed topologi

300 Ssz1p is degraded in zuo1Delta [psi-] cells, but not if the cells carry any of several [