ライフサイエンスコーパス: vacant

1 metric unit, leaving the third Asn67 residue vacant.

2 in the N-domain despite sites I and II being vacant.

3 leaving the innermost portion of the pocket vacant.

4 ntial delta-bond using the psi(4) orbital is vacant.

5 er axial ligand; the lower-axial position is vacant.

6 eaving poorer quality, less successful sites vacant.

7 ination site at the chelated metal virtually vacant.

8 d in the reduced state with the proline site vacant.

9 r in SC samples with more Fe atoms occupying vacant 4d sites is found to be closely related to the de

10 ABCE1/Pelota/Hbs1 also dissociated vacant 80S ribosomes, which stimulated 48S complex forma

11 ichia coli 70S ribosomes, is also present in vacant 80S ribosomes.

12 with the 60S subunit leads to an increase in vacant 80S ribosomes.

13 Nelfinavir stabilizes vacant 80S ribosomes.

14 angiogenin is activated by ribosomes with a vacant A site, the abundance of which increases during c

15 t competition with each other; ISR prefers a vacant A site, whereas RQC displays no preference.

16 mation provides a suprafacial combination of vacant acceptor and donor orbitals that permits this dir

17 trimer of ATR and that binding of ATP to the vacant active site triggers ejection of 1 equiv of AdoCb

18 in filaments with heads leads to the lack of vacant adjacent sites on a filament and a consequent pre

19 ye molecules render higher concentrations of vacant adsorption sites which can accommodate an additio

20 Balon occupies the ribosomal A site in both vacant and actively translating ribosomes in complex wit

21 occurring under the same conditions for the vacant and guest-loaded framework.

22 y complex binds to the A-site whenever it is vacant and the P-site has peptidyl-tRNA; and association

23 erence between the EF-G.GTPase activities of vacant and translocating ribosomes, which are otherwise

24 Differences between the conformations of vacant and tRNA-bound 70S ribosomes suggest an induced f

25 tate-owned foreclosures, which typically sit vacant, and foreclosures purchased by third-party buyers

26 bonds at the tips of the branches to create vacant areas for functionalization with a different thio

27 owever, approximately 400 positions remained vacant at the end of the hiring season, with groups stil

28 critical part of the binding site is already vacant because of spontaneous peptide motion.

29 dmission paper registration), logistical (no vacant beds, no physician available), and process-based

30 via delocalization of radical character into vacant boron p-orbitals, but that hyperconjugation of te

31 e evidence that these 80 S complexes are not vacant but contain mRNA that is stably bound to the 40 S

32 51N structure, the third metal site was also vacant, but the phosphate anion bound closer to the surf

33 ing site, partially occupying the space left vacant by the departing molecule (substrate or cofactor)

34 When compound 4, which has a vacant C(4) B(2) O(4) cavity, is reacted with sodium tet

35 is issue, we determined the structure of the vacant C. albicans 80S ribosome at 2.3 angstroms and its

36 om the occupied CH2/NH/O p pi orbital to the vacant C=C pi* LUMO of the SWNT.

37 rather than by a specific interaction at the vacant Ca(2+)-binding site.

38 One sub-unit showed no bound ligand and a vacant calcium site close to a crystal contact.

39 tetramerize on a nucleosome, generating two vacant CD sticky ends.

40 ve) by cells containing honey and (below) by vacant cells containing air.

41 Up to five vacant cells in the brood region can be occupied by cell

42 is precluded from binding cognate DNA at the vacant cleft.

43 orm conjugates of moiety-occupied and moiety-vacant concentration states of metabolites and cofactors

44 must enter the coordination sphere from the vacant coordination position trans to the Re=O group, a

45 The vacant coordination site and low valence of (C(5)H(4)SiM

46 These incorporate a vacant coordination site at each Cu(II) center and have

47 attractive Coulombic occlusion of the fourth vacant coordination site at Pd/Pt centers by the Cr(CO)3

48 ation of a selenocysteine ligand to create a vacant coordination site for catalysis and close by cons

49 in the reaction media, thereby generating a vacant coordination site for catalysis.

50 n, dnHEM1, with an axial histidine ligand, a vacant coordination site for generating reactive interme

51 er, and catalysis involves H2 binding on the vacant coordination site of an iron centre.

52 Azide binds weakly at the vacant coordination site of reduced SOR to give a coordi

53 en monodentate phosphine ligands are used, a vacant coordination site on nickel creates an extra Ni-O

54 the corresponding kappa(1)-forms featuring a vacant coordination site sit only slightly higher in ene

55 ich the sterically crowded quadrants flank a vacant coordination site, exemplified by the crystal str

56 aturated polyamine metal complexes and whose vacant coordination sites can be occupied by anion donor

57 onium-based MOF (Zr-MOF) that contains three vacant crystallographically defined coordination sites.

58 e filled pai* orbitals of (C(6)H(6))(4-) and vacant d(xy) and d(x(2)-y(2)) orbitals of the Ln(3+) ion

59 roxidases have a five-coordinate heme with a vacant distal coordination site that permits the iron ce

60 l has been proposed in which NO binds to the vacant distal face to form a transient six-coordinate he

61 he Tyr67-oxidized/carbonylated protein has a vacant distal ligation site, and it represents the true

62 omains of both predators consistent with the vacant domain hypothesis.

63 In ribosomes with a vacant E site, the L1 stalk is observed either in the fu

64 e combined host and endosymbiont can exploit vacant ecological niches and occupy novel environments [

65 -terminal domain of eIF5 fails to occupy the vacant eIF1 position, and eIF2beta becomes flexible.

66 late, and then placed on the same or another vacant endplate site to form a 'reconstructed' one-bouto

67 ate lifetimes, enabled by the combination of vacant, energetically accessible heterocycle-based accep

68 sing a pair of [4Fe-4S]-like clusters, and a vacant FeMoco site.

69 As land use leaves massive tracts of land vacant for recovery, restoration must undergo a substant

70 valents (FTEs) for family physicians and 376 vacant FTEs for registered nurses.

71 There were 428 vacant funded full-time equivalents (FTEs) for family ph

72 e base of the dinucleotides interacts with a vacant G-triad, forming four additional Hoogsteen hydrog

73 the guanine base of the dinucleotide and the vacant G-triad, which acts as an anchor point of binding

74 fter releasing its TA protein cargo, the now-vacant Get3 recycles back to the cytosol concomitant wit

75 0(3) cm(-3)), the lowest when the homes were vacant (GM: 6.1 x 10(3) cm(-3)) or the occupants were as

76 aign) and (2) a single-family residence when vacant (H2 campaign).

77 ly tethered to the H3-H4 tetramer, while the vacant H2A-H2B site is occupied by the histone-binding d

78 The escaped Milu searched for vacant habitat patches as "stepping stones" and establis

79 m recovering populations and reintroduced to vacant habitats can reestablish populations despite the

80 to the minor population of the hemoglobin's vacant hemes in a cooperative manner, nitrosylates hemog

81 Each family moves to each vacant house at rates that depend on their happiness at

82 al setting), residing in an area with a high vacant housing rate, residing in an area far from an Alc

83 r without cell division and can leave behind vacant HSC niches.

84 el activity patterns of predators may create vacant hunting domains that reduce costly trade-offs for

85 We tested whether this provides vacant hunting domains, places and times where and when

86 (and sometimes occupy a Mn(2+)(A) site found vacant in the native enzyme) and maintain a conserved ar

87 ting and positions offered, filled, and left vacant in the retina fellowship match from 2014 to 2019.

88 pating, positions filled, and positions left vacant in the retina fellowship match increased from 101

89 dral and octahedral sites that are nominally vacant in their ordered counterparts.

90 gation of ACV to the iron centre, creating a vacant iron coordination site into which dioxygen can bi

91 SSPV significantly increases agricultural or vacant land value by about 19.4% within a 2-mile radius,

92 tes to 2400 vacant parcels, we estimate that vacant lands citywide may cumulatively infiltrate 51-54%

93 (CUS) or open coordination sites (OCS) when vacant Lewis acid sites on the metal ions or cluster nod

94 adjacent to the stained region created by a vacant LH1beta.

95 directly to either Mn(2+) or Mg(2+), and the vacant ligand position is occupied by a water molecule.

96 e-in-differences analysis of the impact of a vacant lot greening program in Philadelphia, Pennsylvani

97 Regression-adjusted estimates showed that vacant lot greening was associated with consistent reduc

98 gression-adjusted estimates also showed that vacant lot greening was associated with residents' repor

99 Vacant lot infiltration rates vary widely (0.001 to 5.39

100 proportion of the dogs were observed in the vacant lots (46.2%).

101 OR, 0.09; 95% CI, 0.01-0.88), and maintained vacant lots (OR, 0.17; 95% CI, 0.03-0.81) were significa

102 Our findings differentiate vacant lots as purposeful landscapes that can alleviate

103 Once greened, vacant lots may reduce certain crimes and promote some a

104 To investigate this, we evaluate how vacant lots modulate citywide hydrologic partitioning by

105 were compared with matched groups of control vacant lots that were eligible but did not receive treat

106 Across 4 sections of Philadelphia, 4,436 vacant lots totaling over 7.8 million square feet (about

107 nd "after" outcome differences among treated vacant lots were compared with matched groups of control

108 habitat features (e.g., parks, golf courses, vacant lots).

109 th significantly increased overdose odds had vacant lots, abandoned buildings, alleys, restaurants, a

110 tion InI2(+), which is unusual in having two vacant low-lying p-orbitals.

111 c studies, the entering ligand Y attacks the vacant lower axial coordinate site trans to O, and the r

112 Although the vacant lower axial site in the rhenium complex is the si

113 se sites are assigned to Ca2+ binding to the vacant Mn sites.

114 1sigma(g)(2)1pai(u)(2)1pai(g)*(2) with four vacant molecular orbitals (1sigma(u)*, 2sigma(g), 1pai(u

115 fferent edge surface reactive sites of a cis-vacant montmorillonite layer using first-principles mole

116 ility of the edge surfaces of trans- and cis-vacant montmorillonites.

117 structures demonstrate how ArfA 'senses' the vacant mRNA tunnel and activates RF2 to mediate peptide

118 nserting its C-terminal alpha-helix into the vacant mRNA tunnel.

119 cyst complementation approach that creates a vacant niche in chimeric hosts, enabling the initiation

120 to exploit open resources, however, because vacant niches are generally challenging to identify in p

121 stimulate evolutionary divergence to exploit vacant niches if character displacement results from the

122 tion, changing over time the distribution of vacant niches to which species adapt [2], altering evolu

123 in body size as extinction survivors filled vacant niches.

124 available to compete with H(+) transfer to a vacant, nucleophilic Fe site: had H(+) transfer already

125 ants suggests that the dopants reside in the vacant octahedral locations within the alumina lattice,

126 bosomal peptidyltransferase P-site, which is vacant only prior to the formation of the first peptide

127 16-A resolution structures of RPPs bound to vacant or nontranslating ribosomes.

128 units, the sixth coordination site is either vacant or occupied by solvent molecules.

129 in the transition state between the carbene vacant orbital with the adjacent Si-C sigma-orbital is p

130 ssessing both a lone pair of electrons and a vacant orbital, reminiscent of singlet carbenes.

131 g a lone pair of electrons and an accessible vacant orbital, singlet carbenes resemble transition met

132 asses the consideration of both occupied and vacant orbitals [global molecular orbital contributions

133 bital interactions involving the substituent vacant orbitals and the occupied orbitals associated wit

134 erlap and correlate with the energies of the vacant orbitals of the dienophiles, the lower reactivity

135 lained by electronic stabilization involving vacant orbitals of tricoordinate boron atoms.

136 stabilization and steric protection to both vacant orbitals on the central carbon atom, paving the w

137 ectrophilicity, and possesses two accessible vacant orbitals.

138 elocalization of their spin density into the vacant p orbital of a boron substituent.

139 between the occupied sigma(C-X) bond and the vacant p(pi) orbital on boron is correlated to the elect

140 air from a planar phosphorus centre into the vacant p-orbital at arsenic; the bonding in 2 has been p

141 delocalization of the N lone pairs into the vacant p-orbital at carbon (or a heavier Group 14 elemen

142 ization of the phosphorus lone pair into the vacant p-orbital at germanium.

143 h a hyperconjugative interaction between the vacant p-orbital of these carbenes and the adjacent C-Si

144 Boronic esters with vacant p-orbitals have a significant stabilizing effect

145 inct conformations, corresponding to the E/E vacant, P/E hybrid, and classical states.

146 ng of the unpaired electron in the partially vacant pai orbital (from ionization) with the two other

147 ion from the 1s(C) core orbital to the fully vacant pai* orbitals.

148 d vegetative characteristics associated with vacant parcels and introduced by demolition may absorb r

149 Extending field estimates to 2400 vacant parcels, we estimate that vacant lands citywide m

150 Herein, the Ga and Sb atoms co-occupy the vacant Pb sites, unlike in the case of traditional singl

151 with low-frequency oscillations here termed vacant, perturbed consciousness (VPC).

152 hosphorus atom, eliminating overlap with the vacant phosphorus d-orbitals despite the near-perfect in

153 ction between the nitrogen lone pair and the vacant pi* orbital.

154 n of hydrocarbon chains and concentration of vacant pockets (voids) in the lipid bilayer are thus red

155 en activator inhibitor PAI-1, we blocked the vacant position 4 in beta-sheet A of this serpin with an

156 e that 80% of microbiology laboratories have vacant positions and that filling these positions is cha

157 ed-and feared-consequences are the 40 to 70% vacant posts in residencies of critical care.

158 test whether the SRP receptor (SR) locates a vacant protein translocation channel by interacting with

159 sixth coordination site of the heme-iron is vacant, providing a dioxygen-binding site that would als

160 In the KA-H group, by contrast, the vacant region beneath tall hair cells remained evident e

161 ve characteristics previously attributed to "vacant ribosomal couples," including lability in 500 mM

162 ing single-turnover EF-G-dependent GTPase on vacant ribosomes and to elucidate the mechanism by which

163 Vacant ribosomes may provide a means to exclude ribosome

164 ented by omission of EF-Tu, or in studies on vacant ribosomes.

165 olution structures of ribosomal subunits and vacant ribosomes.

166 Vacant sequons have another opportunity for glycosylatio

167 ramolecular G-quadruplexes: one containing a vacant site (4n - 1) and the other with an unbound guani

168 The vacant site 2 causes partial induction of mtsABC, indica

169 ional DNAs indicate that the presence of the vacant site and the activity of the functional DNAs are

170 The vacant site approach demonstrated here can be used to de

171 ional DNA sensors using unmodified DNA via a vacant site approach is described.

172 rates in two sites attract each other into a vacant site between them and b) when substrates in adjac

173 When the vacant site binds ATMND, ATMND's fluorescence is quenche

174 of yet a third line, Mo17, because the HelB vacant site is deleted in B73.

175 bl synthesis and where binding of ATP to the vacant site leads to the transfer of the high value AdoC

176 Each bird may choose a vacant site or challenge an occupier for its site.

177 By extending one end of DNA with a loop, a vacant site that binds an extrinsic fluorophore, 2-amino

178 (4)]; L/L' = pyridine, pivalonitrile, or the vacant site, BAr(4)(F) = B[(3,5-(CF(3))(2))C(6)H(3)](4))

179 er; the loser incurs a cost and must go to a vacant site.

180 ne guanine in the G-tetrad core, harboring a vacant site.

181 (TS) with X in an axial position trans to a vacant site.

182 Control experiments using vacant-site-free DNA duplexes and inactive variants of t

183 with motor neurons and their functions, and vacant sites (or vacancies) devoid of tSCs and axons pro

184 xons rapidly reverse fate and grow to occupy vacant sites at a neuromuscular junction after laser rem

185 rationalizes the experimental data: two such vacant sites at the metal are needed to allow coordinati

186 m breeding by competition which quickly fill vacant sites following periods of low adult survival.

187 y facilitated by the identification of their vacant sites in Helitron-minus lines.

188 Saturation of the vacant sites in the 16- and 14-electron complexes with c

189 Ag, when introduced into CBB, occupies vacant sites in the spacer region, forming octahedral co

190 t that the peptides preferably interact with vacant sites of the face-centered cubic lattice above th

191 While the Ni-Fe' derivative has vacant sites on both metals for hydride formation, the u

192 y interaction of the histidines with the two vacant sites on Ni(II) ions chelated to the surface NTA

193 ve elimination of Bu(t)3SnH from 1 to afford vacant sites on the Pt center, thus facilitating the exc

194 levant irreversible O(2) activation steps on vacant sites present within saturated CO monolayers.

195 , this study proposes the utilization of the vacant sites remaining unoccupied after dye uptake satur

196 als stems from facile alkane coordination at vacant sites, enabled by the overall lability of the lig

197 ice oxygen, through occupying surface oxygen-vacant sites, rather than Fe redox chemistry, which chal

198 ion near the parent tree and colonization of vacant sites, the locations of which are unpredictable i

199 ending and phosphine loss help to create two vacant sites, thus triggering the high hydrogenation act

200 ics model allowing for ideal, defective, and vacant sites.

201 te due to the stronger sorption of Cd at its vacant sites.

202 in a distorted octahedral geometry with two vacant sites.

203 additional factors such as the absence of a vacant sixth coordination site sufficiently accessible f

204 the increasing detection resolution, in the vacant space between two energy levels of a given resona

205 By pre-empting vacant space, overgrowing corals, deterring the settleme

206 ty size increases beyond the capacity of the vacant space, the formation of multiple acceptor-type Cu

207 nit cell, containing a significant volume of vacant space.

208 Quantification of vacant spines as compared to those on boutons revealed a

209 the number of synaptic spines increased and vacant spines decreased drastically.

210 ns and atypical Purkinje cell dendrites with vacant spines.

211 its neighbors compete to reproduce into the vacant spot.

212 DBS induced episodes of abnormally long, vacant staring with low-frequency oscillations here term

213 Bilayer lines could be formed within the vacant strips by vesicle fusion.

214 The width of vacant strips could be controlled down to 15 nm.

215 range of carboxylic acids by filling up the vacant substrate access channel of the photodecarboxylas

216 Concurrently, the protease was adsorbed to vacant surface sites at the iron oxides, which significa

217 tectable in a subset of transgenic boutons ("vacant synapses") with diminished levels in the remainde

218 sed on axonal sprouting and occupancy of the vacant synaptic space due to deafferentation is the base

219 Two distinct vacant tetrahedral sites were identified at the end of t

220 of the interfacial lattice sites need to be vacant to explain the observed mixing.

221 Greening of vacant urban land may affect health and safety.

222 , peripheral flanges, and fits snugly into a vacant vertex site.

223 ers reassemble in vitro into procapsids with vacant vertices called "whiffleballs".

224 n(4+) layer cation sites in SP6-MnO(x)() are vacant, whereas the analysis of the XANES suggests that

225 (R)2 is fully occupied and operator O(R)3 is vacant, wild-type lambda cI activates transcription from

226 Here, we report the structure of the vacant yeast uL3 W255C mutant ribosome by X-ray crystall

227 e converted to a structure incorporating one vacant Zr site and one terminal OH group per face by rea