ライフサイエンスコーパス: stoichiometry

1 e in subunit composition and vary in subunit stoichiometry.

2 ct to the well-described features of the 1:1 stoichiometry.

3 n states with well-defined protein-metal ion stoichiometry.

4 ss, in contrast to the assumed 3:1, in a 2:2 stoichiometry.

5 duced by fractionally changing the precursor stoichiometry.

6 he characterization of their composition and stoichiometry.

7 receptors of defined subunit composition and stoichiometry.

8 nscripts and a disturbance of linker histone stoichiometry.

9 iron oxide with an unconventional Fe(5) O(6) stoichiometry.

10 ncentration-dependency of UBAN/di-Ub binding stoichiometry.

11 rfering ions each form complexes of only one stoichiometry.

12 3 forms heterohexamers with CcmK4 with a 1:2 stoichiometry.

13 biological significance by evaluating their stoichiometry.

14 the formation of complexes with a 2:1 Gag/NA stoichiometry.

15 pulations with random and diverse chromosome stoichiometry.

16 hanges in their expression, trafficking, and stoichiometry.

17 of A (a)Mn(II) (b)(CN) (a+2 b) (A = cation) stoichiometry.

18 metric forms of the CCNC that vary in CENP-N stoichiometry.

19 a 1:1 (antibody:myostatin homodimer) binding stoichiometry.

20 ss, in contrast to the assumed 3:1, in a 2:2 stoichiometry.

21 tion with reducing sugars at the desired 1:1 stoichiometry.

22 pitch black by controlling its degree of non-stoichiometry.

23 has been limited due to low labeled peptide stoichiometry.

24 sin complexes (REC-8 and COH-3/4) in defined stoichiometry.

25 ntailing the formation of a complex with 1:1 stoichiometry.

26 gth representations hand-engineered from the stoichiometry.

27 in intensity with sintering temperature and stoichiometry.

28 tifacts and perturbations of protein complex stoichiometry.

29 imum zone and consequent changes in nutrient stoichiometries.

30 also detected a polydisperse distribution of stoichiometries.

31 do not compromise the accuracy of calculated stoichiometries.

32 on channels assembled with incorrect monomer stoichiometries.

33 r crystal structures or of tuning mobile-ion stoichiometries.

34 ) Fe(3-) (x) O(4) thin films with controlled stoichiometry, 0 <= x <= 2.3, and lattice strain are gro

35 binding constant (10(4) L mol(-1)), complex stoichiometry (1:1), and thermodynamic potential for BSA

36 nal outcomes and involving different protein stoichiometries: (1) simple exchange of proteins and (2)

37 rts the environmental pollutant perchlorate (stoichiometry 1Na(+):1ClO(4)(-)), which competes with I(

38 brane protein that actively transports I(-) (stoichiometry 2Na(+):1I(-)) in thyroid physiology and ra

39 Nutrient stoichiometry affects eco-evolutionary feedbacks in ways

40 Allostery, topology, and building block stoichiometry all play important roles in the efficacy o

41 Tuning the reagent stoichiometry allows for semi- and complete hydrogenatio

42 ides a novel parameter a whose dependence on stoichiometry allows one to quantitatively interpret the

43 Decoding the precise protein stoichiometry allows us to develop an organisational mod

44 This manipulation of nutrient stoichiometry altered the stability of host-parasite int

45 Using a 1:1 stoichiometry, an alternating (AB)(n) structure is produ

46 When restoring stoichiometry, an enhanced ferromagnetic insulating stat

47 major challenge because of unknown labeling stoichiometries and complex fluorophore photophysics.

48 to reveal time- and concentration-dependent stoichiometries and conformations of assembling human Mu

49 Fe-S clusters with different iron-to-sulfur stoichiometries and distribute these clusters to appropr

50 re-to-ionic site ratios, considering complex stoichiometries and ion charges.

51 = 3, b = 5) series possessing unprecedented stoichiometries and lattice motifs.

52 of the subsequent NPNA and, hence, different stoichiometries and modes of antibody binding to rsCSP.

53 diluted UCNP dispersions including particle stoichiometries and size distributions.

54 described functionally and structurally, the stoichiometry and arrangement of heteromeric Cx channels

55 which the hump occurs, are determined by the stoichiometry and chromophoricity of the hydrological in

56 de/bromide ratio compared with the precursor stoichiometry and consequently a reduction in the band g

57 This analysis reveals the stoichiometry and contact interfaces between the key pro

58 We show that stoichiometry and cooperativity is a function of DNA len

59 Interestingly, the stoichiometry and diffusion properties of the wild-type

60 ions regarding correlations between apparent stoichiometry and dwell times of condensates to being pr

61 alysts by controlling the chalcogen or metal stoichiometry and explore critical aspects of the hydrog

62 ely heavily on intricate control of material stoichiometry and generally suffer from toxic and comple

63 The relationships among fungal stoichiometry and growth disappeared in more complex med

64 rocyclic hosts exhibit a rare 2:1 host-guest stoichiometry and guest-dependent slow or fast exchange

65 The composition, stoichiometry and interactions of supramolecular protein

66 life-cycle inventory framework that couples stoichiometry and kinetics to obtain site-specific water

67 Parameters such as photon stoichiometry and light intensity are highlighted within

68 L native thick filaments in which the MyBP-C stoichiometry and localization are preserved, native thi

69 ved and mobile associations to measure their stoichiometry and mobility and analyzed data from experi

70 ired for ribosome maturation, normal 18S/28S stoichiometry and modulated the translation of mitochond

71 microscopy, to decipher the absolute protein stoichiometry and organizational variability of single b

72 this study, CDMS is used to characterize the stoichiometry and population distribution of antibodies

73 results support that SHR-SCR protein complex stoichiometry and regulation of SHR transcription modula

74 bosomes with distinct ribosomal protein (RP) stoichiometry and regulatory roles in protein synthesis

75 n eukaryotic NER, although reports about its stoichiometry and role in damage recognition are controv

76 interactive effects of time since fire, soil stoichiometry and spatial distance in the reassembly of

77 nalyzing nine response variables of nutrient stoichiometry and stable isotopes per coral fragment, we

78 Such synergistic control of stoichiometry and structure at the reactive interface pr

79 These are the first to resolve the stoichiometry and structure of the core.

80 some parameters such as solvent, others like stoichiometry and temperature still required further opt

81 evealed that the three subunits have a 1:1:1 stoichiometry and that nearly 100% of them are present i

82 ndings demonstrate the utility of ecological stoichiometry and the importance of ionome-wide data in

83 results highlight the importance of subunit stoichiometry and the presence or absence of specific ac

84 Herein, we describe measurements of stoichiometry and thermochemistry for hydrogen bound to

85 treams because of its variable degree of non-stoichiometry and thus develops a 'chemical memory' that

86 rboxysomes and their structural composition, stoichiometry, and adaptation to cope with environmental

87 systems approach, elemental carbon-nitrogen stoichiometry, and biomarker scaling, to demonstrate a s

88 ncluding state dependence, G311 sensitivity, stoichiometry, and central cavity accessibility.

89 jection, electron/ion beams, thermal loss of stoichiometry, and chemical treatments or by a combinati

90 of post-translational modifications (PTMs), stoichiometry, and conformational changes induced by lig

91 se methods enable us to probe the structure, stoichiometry, and domain interactions in the ~240 kDa B

92 nation of the complexation constant, complex stoichiometry, and percentage of free/bound drug, due to

93 rfaces of RNA/protein complexes of different stoichiometry, and provides a detailed understanding of

94 olecules with a range of binding affinities, stoichiometry, and size-scales.

95 the roles of resource availability, nutrient stoichiometry, and soil abiotic factors in driving below

96 The identity, stoichiometry, and stability of these interactions chara

97 The composition, interactions, stoichiometry, and topological organization of proteins

98 These unusual structures and stoichiometries are attributed to the very ionic nature

99 suggest that MCUB-dependent changes in mtCU stoichiometry are a prominent regulatory mechanism to mo

100 nium carbide (ZrC(x)) with sample purity and stoichiometry are still not understood due to discrepanc

101 al reactions can effectively follow nonunity stoichiometries as can be found in the electrochemistry

102 achine learning approach that takes only the stoichiometry as input and automatically learns appropri

103 sed strategies, is used to determine subunit stoichiometry as well as cofactor and lipid binding.

104 hrough the NMR determination of complexation stoichiometry, association constants, and stereochemical

105 at O-fucosylation sites and variable mannose stoichiometry at C-mannosylation sites.

106 alysis showed that O-fucose occurred at high stoichiometry at most consensus sequences of NOTCH2 and

107 odified with the GlcFuc disaccharide at high stoichiometry at O-fucosylation sites and variable manno

108 molecular interactions and quantify subunit stoichiometry at the single molecule level.

109 The most widely used assays for GPCR stoichiometry, based on resonance energy transfer, are u

110 ulations, which suggest that the 2:1 binding stoichiometry between alpha-cyclodextrin and Au(CN)(2)(-

111 A 1:1 binding stoichiometry between Au(CN)(2)(-) and alpha-cyclodextri

112 A 2:1 stoichiometry between macrocycle and diphosphate produce

113 diffraction, which demonstrates the rare 2:2 stoichiometry between the anionic phosphonate end groups

114 ing of the rotor, and proposed mismatches in stoichiometry between the two rings have long provided a

115 ble of interconverting complexes of variable stoichiometries, binding energetics and WW domain occupa

116 degradation and perturbed ribosomal subunit stoichiometry, both of which were rescued by a single K2

117 d template/primer DNA binding affinities and stoichiometries by Pol delta in the absence of PCNA, usi

118 Notably, the differences in H(2) :N(2) stoichiometry by alternative nitrogenases (~1.5 for V-ni

119 also demonstrate precise control over metal stoichiometry by tuning the concentration of metal salt

120 nitride framework with a remarkable 3:5 C:N stoichiometry (C(3)N(5)) and an electronic bandgap of 1.

121 s it is known that each aneuploid chromosome stoichiometry can give rise to a distinct pattern of gen

122 The predominant form, with the stoichiometry Cas1(8)-Cas2(4)-Csn2(8), referred to as mo

123 ifunctional reactants in systems with varied stoichiometries, catalyst, and loadings.

124 Departure from stoichiometry changes the thermo-physical response of th

125 ons, and ribosomal proteins, including their stoichiometry, compositions, paralogues, and posttransla

126 rotein trimer of 42 kDa was detected and its stoichiometry confirmed by higher energy collision disso

127 e, we demonstrate the first example of using stoichiometry-control to specify the monomer sequence in

128 the hexon cavity, and clarifies the hexon:VI stoichiometry conundrum.

129 commitment that integrates temporal protein stoichiometry data with mRNA measurements.

130 usters, rendering N-WASP and Arp2/3 activity stoichiometry dependent.

131 Instead, stoichiometry-dependent competition between protein netw

132 enhances I (Ks) activity in both a dose- and stoichiometry-dependent fashion by changing the slowly a

133 namic acid can enhance I (Ks) in a dose- and stoichiometry-dependent fashion, regulated by its intera

134 Here we have found that AMPARs show a clear stoichiometry-dependent modulation by the prototypical T

135 references of nucleotide sequences and their stoichiometry determine the 3'-splice site.

136 ne-induced upregulation and changes in nAChR stoichiometry differ across brain regions.

137 FT and GT to deconvolve the charge state and stoichiometry distributions of polydisperse ions.

138 ods to determine charge states and detergent stoichiometry distributions.

139 e of stable uranium oxides with intermediate stoichiometries (e.g., U(3)O(8)) and sensitivity of the

140 er the complex is formed or not, NMR for the stoichiometry elucidation, and UV-visible spectrophotome

141 number of potential subunit arrangements and stoichiometries, even when only combining two Cx isoform

142 , little is known about the effect that this stoichiometry exerts on certain AMPAR properties.

143 Different binding stoichiometries found upon titration with metal ions cor

144 ng season on seed yield, nutrient uptake and stoichiometry from 2001 to 2017.

145 nsillar B cells, we found that tunable DM/DO stoichiometry governs DM(free) activity for exchange of

146 High binding stoichiometry (H:G(2)) was observed for all CPA protonat

147 The reaction of HNO with RSSH at varied stoichiometries has been examined with the observed prod

148 ts different anion substrates with different stoichiometries has remained unelucidated.

149 Hexon:VI stoichiometry has been uncertain, and only fragments of

150 4)O(5), Fe(5)O(6), Fe(7)O(9), and Fe(9)O(11) stoichiometry has raised questions about their existence

151 Here, we identify protein complex stoichiometry imbalances as a major cause of protein agg

152 ng the large design space of gene expression stoichiometries in mammalian cells using current methods

153 ms and post-translational modification (PTM) stoichiometry in Alzheimer's disease (AD), we generated

154 reversible electrode processes with complex stoichiometry in cyclic voltammetry (CV) at macroelectro

155 of nicotine on the distribution of receptor stoichiometry in different mouse brain regions.

156 spectrometry (nTDMS) to determine the copper stoichiometry in each pMMO subunit and to detect post-tr

157 findings highlight the utility of ecological stoichiometry in illuminating the mechanisms that couple

158 ion experiments indicated that the prevalent stoichiometry in solution is 4 TreS + 2 Pep2 protomers.

159 identifies heteroprotein complexes and their stoichiometry in the NE by accounting for spectral cross

160 remarkably facilitated by a localized 16-mer stoichiometry in the periplasmic-most coupling domain of

161 ce seed yield, nutrient uptake, and nutrient stoichiometry in the plant.

162 onfirm that the CPSF30-hFip1 complex has 1:2 stoichiometry in vitro.

163 identify and characterize distinct ribosome stoichiometry in yeast and mammalian systems.

164 e results were analysed as a function of the stoichiometry, in which both crystalline structures show

165 h 70% of replication forks, with a hexameric stoichiometry, indicating maximal occupancy of the singl

166 Binding of ligelizumab to IgE in a 2:1 stoichiometry induces an extended and twofold symmetrica

167 -mass spectrometry, which provides shape and stoichiometry information.

168 subunits by elucidating their conformation, stoichiometry, interacting fraction, and affinities in l

169 oretical explanation, that the B-site cation stoichiometry is crucial for the creation and control of

170 affect SC formation or activity, and that SC stoichiometry is dictated by the level of CIII/CIV biosy

171 te sensing-based metrics that rely on tissue stoichiometry is limited due to their strong dependence

172 Outer kinetochore stoichiometry is remarkably plastic and responsive to mi

173 e crystal with a small deviation from oxygen stoichiometry is studied.

174 rison with most other cuprates, has a stable stoichiometry, is largely free of defects and may be reg

175 he potassium cation (K(+) ) with 1:1 binding stoichiometry (K(a) =6.6x10(5) m(-1) ).

176 Reduction of H1 stoichiometry leads to decreased H3K27 methylation, incr

177 poration and its correlation with the cation stoichiometry leads to the formation of a solid solution

178 that AMPARs can bind to TARPs with variable stoichiometry, little is known about the effect that thi

179 ored stoichiometries that optimized binding (stoichiometry matching) but still were quite broad.

180 des artificially mixed at low heavy-to-light stoichiometry measured using standard data dependent acq

181 Importantly, misinterpreted stoichiometries misguide the design of new ionophores an

182 s formed avid homo-oligomers with high-order stoichiometry (n > 2 protomers per homo-oligomer), but i

183 Loads, concentrations, stoichiometry (N:P), and bioavailability (percentage dis

184 Because CIII can neither lower its pumping stoichiometry nor transfer protons completely across the

185 be molecularly programmed to display precise stoichiometries of any desired PAMP.

186 we have, for the first time, determined the stoichiometries of complexes formed between alphaBc and

187 In this study, a range of stoichiometries of hot-pressed ZrC(1-x) were examined by

188 By examining the dispersity and stoichiometries of these complexes over time, and in res

189 f a complex metal M oxide (M (4)O(5)) with a stoichiometry of (Fe(3+) (2.15)Fe(2+) (1.59)Ni(2+) (0.17

190 es interactions between DMS3 and DRD1 with a stoichiometry of 1 DRD1:4 DMS3:2 RDM1.

191 and H(+) transport and displayed an altered stoichiometry of 1.6:1.

192 The structure reveals a unique stoichiometry of 1:1 and 2:1 (DSG2: knob trimer) not pre

193 uplex unfolding, with a final complex with a stoichiometry of 2 POT1 per 24 nt DNA.

194 erization of the labeled antibody revealed a stoichiometry of 21 Nd atoms per antibody molecule that

195 Dnmt3b3 forms a complex with Dnmt3a2 with a stoichiometry of 2:2.

196 a4- and alpha2-containing receptors with the stoichiometry of 2alpha:3beta subunits but not low sensi

197 Our results indicate a dominant subunit stoichiometry of 3Cx26:3Cx30 with the most abundant subu

198 olving mechanisms of CaM-Ca(V) feedback, the stoichiometry of CaM interaction with Ca(V) channels rem

199 ased on this, and on the 4:2 (SSDP-Chip/LDB) stoichiometry of ChiLS, we derive a highly constrained s

200 gical experiments to show that the different stoichiometry of ClO(4)(-) transport is due to ClO(4)(-)

201 pMMO-nanodisc complexes with a higher stoichiometry of copper-bound PmoC exhibit increased act

202 uide RNA (sgRNA) that enables the controlled stoichiometry of CRISPR components and limits the possib

203 By changing the sequences and stoichiometry of DNA anchors, we can control the amount

204 s and link these effects to the affinity and stoichiometry of each antibody for monomeric and fibrill

205 The precise stoichiometry of each component that permits this sequen

206 taining SAs by Fe(VI) and alter the reaction stoichiometry of Fe(VI) and SA from 4:1 to 3:1.

207 The ATPase activity of VCP modulates the stoichiometry of HUWE1 in the Shoc2 complex as well as H

208 tition but also, critically, by changing the stoichiometry of I(-) transport to 1:1, which greatly re

209 )-Thr(369) (P2-P1) reactive site bond with a stoichiometry of inhibition of 3.8 and an association ra

210 any multimeric complex by investigating the stoichiometry of Kv2.1/Kv6.4 channels.

211 Based on the reported 3:1 stoichiometry of Kv2.1/Kv9.3 channels, we tested the hyp

212 ramifications of the non-arbitrary elemental stoichiometry of life; and maximization of limiting reso

213 ocalization may be used to study the subunit stoichiometry of membrane receptors.

214 rties, chemical boundary conditions, and the stoichiometry of metabolic pathways, regardless of the p

215 ty increased, and significantly modified the stoichiometry of mobilized elements.

216 tructures and avoids the need to control the stoichiometry of multiple distinct units.

217 n in the IP(3)R structure, as well as on the stoichiometry of mutant subunits assembled within the te

218 ut rather to a beneficial rebalancing in the stoichiometry of myelin lipids and proteins.

219 ults converge on a model in which an unusual stoichiometry of non-motor subunits controls dynein-2 as

220 nts and test whether such differences in the stoichiometry of nutrient supply propagate through plant

221 Our results suggest the stoichiometry of outer kinetochore submodules is strongl

222 Using bond-valence rules we propose a stoichiometry of Pb(II) binding on the hematite (1102) s

223 l line (trxo1-1) revealed an increase in the stoichiometry of photorespiratory CO(2) release and impa

224 However, through the stoichiometry of primary production, organic carbon buri

225 each responds differently to changes in the stoichiometry of proteins in obligate multi-subunit comp

226 tal determination of the oligomeric state or stoichiometry of proteins remains a nontrivial challenge

227 ith a monodisperse distribution and in a 1:1 stoichiometry of PSEN1 and nicastrin subunits.

228 We obtain accurate stoichiometry of shell proteins and internal enzymes of

229 phase separation is overall regulated by the stoichiometry of SSB and ssDNA.

230 eproducibility, and precision in controlling stoichiometry of targeting peptides.

231 This symmetry mismatch explains the stoichiometry of the complex.

232 embranes are controlled by the stability and stoichiometry of the complexes between the ionophore, L,

233 The relative affinities and stoichiometry of the DIX-DAX interaction provide a mecha

234 opose unambiguous diagnostic criteria of the stoichiometry of the electrode reaction.

235 By analysing changes in the architecture and stoichiometry of the Escherichia coli SMC complex, MukBE

236 easurements are required for determining the stoichiometry of the oligomers.

237 PbI(6) and gamma-CsPbI(3) through tuning the stoichiometry of the precursors between CsI and PbI.

238 ways osmotically balanced, regardless of the stoichiometry of the pump or the ratio of Na+ and K+ con

239 0 kDa can be targeted simply by altering the stoichiometry of the reaction.

240 Here, we quantify the kinetics and stoichiometry of the relevant abiotic reactions in a ser

241 SCR in the QC and CEI which incorporated the stoichiometry of the SHR-SCR complex as well as upstream

242 Dwell time varies with relative stoichiometry of the signaling proteins in the phase-sep

243 The stoichiometry of the two processes was determinative for

244 ) were interpreted based on the kinetics and stoichiometry of the underlying chemical reactions.

245 ssential for HDV replication, and the proper stoichiometry of these complexes could be critical for t

246 How an effective stoichiometry of this many constituent subunits is co-or

247 d expression of TpnT-CD70 in vivo and normal stoichiometry of total TnT in myofilaments of heterozygo

248 coupled plasma (ICP)-MS analysis indicated a stoichiometry of two zinc ions per highly active PPR65 m

249 ts of a systematic modulation of oxygen over-stoichiometry of VO(2) from 1.86 to 2.44 on the band str

250 e RPs, RACK1 and 2 of the 8 RP paralogs, the stoichiometry of which remained constant across differen

251 s study a method is outlined to quantify the stoichiometry of ZrC(1-x) and free carbon phases, provid

252 a method for the accurate measurement of the stoichiometry of ZrC(x) using three independent experime

253 stimated K(D) values in the low uM range and stoichiometry of ~ 8 to ~ 20 galectin molecules binding

254 First, the impact of ion stoichiometry on skin penetration of drugs is assessed u

255 teins and the determination of metal/protein stoichiometry, on the basis of energy dispersive X-ray f

256 The TRPV6-CaM complex exhibits 1:1 stoichiometry; one TRPV6 tetramer binds both CaM lobes,

257 ction of another protein, thus maintaining a stoichiometry optimal for productive infection.

258 matter without compromising the cleanliness, stoichiometry, or mean free path.

259 rboxyl tail switched the apparent functional stoichiometry, permitting two CaMs to mediate functional

260 otein interaction kinetics and estimation of stoichiometries (PIKES) analysis, a systematic proteomic

261 , mRNA, and proteins made by key brain genes-stoichiometry-plays a critical role in defining the clin

262 However, stoichiometry-preserving, purely thermal, reversible pha

263 e-binding sites and may contribute to higher stoichiometry protein N-acylation in vivo.

264 Soil ecological stoichiometry provides powerful theories to integrate th

265 With stoichiometries ranging from [2 Fe:9 Zn:6 protomers] to

266 d by substrate carbon(C) : N and C : (N : P) stoichiometry rather than by substrate N or P.

267 r Waals forces with the binding constant and stoichiometry ratio of 1.88 x 10(5) M(-1) and 1:13, resp

268 wn, exploiting the difference in the binding stoichiometry represents an underexplored avenue toward

269 Orai1-SNP leads to a mis-match in Orai1:STIM stoichiometry, resulting in inhibition of Ca2+ entry and

270 Orai1-SNP leads to a mis-match in Orai1-STIM stoichiometry, resulting in inhibition of Ca2+ entry and

271 In addition to RP stoichiometry, ribosomes host a vast array of protein mo

272 at a composition meets basic requirements of stoichiometry, steric demands, and charge neutrality, re

273 diversity, post-translational modifications, stoichiometry, structural arrangement, stability, and ov

274 STEM-EELS reveals mixed interfacial stoichiometry, subtle lattice distortions, and oxidation

275 ce of two primary ion complexes of different stoichiometries, such as IL (zi) and IL(2) (zi), was rep

276 its expression of NifD and NifK in a defined stoichiometry supportive of activity.

277 -dimensional sp(3)-bonded nanomaterial of CH stoichiometry synthesized from benzene at high pressure

278 we first define a series of space group and stoichiometry templates corresponding to hypothesized co

279 ady-state cluster size distributions favored stoichiometries that optimized binding (stoichiometry ma

280 Within this stoichiometry, the Kv6.4 subunits have to be positioned

281 ng the one fluorophore per molecule labeling stoichiometry, the limit of detection (S/N > 3) and limi

282 +)-binding sites, (ii) determine the binding stoichiometry to be four Ca(2+) per CP heterodimer and e

283 e exclusive formation of complexes of higher stoichiometry unless the ionophore is used in excess.

284 he response of ecosystem to altered nutrient stoichiometry using eddy covariance fluxes measurements,

285 We investigate the Kv2.1/Kv6.4 stoichiometry using single subunit counting and function

286 ter reaction times; (iv) equimolar substrate stoichiometry; (v) expanded sugar scope; (vi) higher sel

287 ) and organic carbon, the formate-to-nitrate stoichiometry was determined as 3.1 +/- 0.2 at neutral p

288 Forty years after the H(+)/e(-) stoichiometry was established, a consensus has yet to be

289 For selecting the most probable stoichiometry, we introduce a model-selection method tha

290 Based on reaction stoichiometry, we quantify a possible impact of calcium

291 s, but various Mg(2+)-bisphosphonate-binding stoichiometries were previously reported.

292 r their habitat use, selective foraging, and stoichiometry, which can in turn affect trophic interact

293 enzymes form a unique heterocomplex with 3:3 stoichiometry, which was confirmed by enzymatic assays,

294 iments, which revealed different PLP-binding stoichiometries with WT and mutant PNPOx forms.

295 The FH sensor coordinates Fe(3+) in a 1:2 stoichiometry with a binding constant, K(a) = 5.25 x 10(

296 ochrome c oxidase (CIV) forms SCs of varying stoichiometry with cytochrome bc (1) (CIII).

297 ) found a strong dependence of anion binding stoichiometry with the solvent employed.

298 FtsX periplasmic domain complex has a 1-to-2 stoichiometry with two distinct FtsX-binding sites locat

299 e at equilibrium for both simple and complex stoichiometries within minutes, as well as the associate

300 , U4, U5, and U6 snRNA, are present in equal stoichiometry within the spliceosome, we found that thei