ライフサイエンスコーパス: stable complex

1 ratio is important to produce a soluble and stable complex.

2 idual gammaTuSC components for maintaining a stable complex.

3 ynthetic enzymes with the cytoskeleton via a stable complex.

4 native mechanism to facilitate assembly of a stable complex.

5 20 conformation of the glycoprotein led to a stable complex.

6 subunit before finally re-entering to form a stable complex.

7 oE, binding of the protein results in a more stable complex.

8 Tah1 binds to the Pih1 C terminus to form a stable complex.

9 f Tah1 to Pih1 allows for the formation of a stable complex.

10 domain binds preferably Cu(II) ion forming a stable complex.

11 s of interaction with heme to form this very stable complex.

12 udies clearly reveal that LumC13-ALK5 form a stable complex.

13 s and physically interact as a biochemically stable complex.

14 ging 'dynamic complex' rather than a typical stable complex.

15 n between these sites are required to form a stable complex.

16 ric-field-induced slow dissociation of these stable complexes.

17 ty, 4oo, produces the most thermodynamically stable complexes.

18 dissociation rates, indicating formation of stable complexes.

19 igands in the binding pocket thereby forming stable complexes.

20 ediates that subsequently relax to specific, stable complexes.

21 bation leading to an increased population of stable complexes.

22 B*0801 and antigenic precursor peptides form stable complexes.

23 sphine 1 with K(2)PtCl(4) afforded the bench stable complex 3 which upon treatment with Ag[CB(11)H(6)

24 results indicate that HO-1 and CYP1A2 form a stable complex and have mutual effects on the catalytic

25 es demonstrated that KLF15 and the GR form a stable complex and that these stress-induced transcripti

26 of two direct repeats is required to form a stable complex and to melt DNA.

27 is essential for the ability of CHT7 to form stable complexes and reverse the cellular phenotypes and

28 o encourage more studies on the dynamics of "stable" complexes and to provide a word of caution about

29 ly interacts with Hha (rather than forming a stable complex) and enhances the spontaneous oxidation o

30 We find the CH3 homodimer to be a highly stable complex, and its dissociation force of >150 pN at

31 CysK and CdiA-CT form a stable complex, and their binding interaction appears to

32 sulted in shortened M-C bond lengths for the stable complexes, and it was found that Fe(nor)4 receive

33 CCL3, CCL4, CCL5, CCL24, and XCL1, extremely stable complexes are formed.

34 he amino-terminal sensor domain is to form a stable complex as a functional kinase, but possibly not

35 e short, conserved promoter sequences form a stable complex at physiological temperatures, and this c

36 s, archaeal Cdc45 and GINS form an extremely stable complex before binding MCM.

37 Formation of a stable complex between clock proteins and CK1 is a conse

38 sipation (QCM-D) resolved the formation of a stable complex between CymA and one of its native redox

39 ecessary, which leads to a thermodynamically stable complex between hnRNP K and the unfolded i-motif.

40 NF-kappaB signaling that the formation of a stable complex between NF-kappaB and the ankyrin repeat

41 RNA and the 3'-overhang of DNA results in a stable complex between p58C and the DNA/RNA duplex.

42 sport model emerging from our data invokes a stable complex between PCATs and their cargo proteins fo

43 inhibitors of alpha-syn aggregation, but no stable complex between the sHsps and alpha-syn was detec

44 in interactions, enabling the formation of a stable complex between these two proteins.

45 which is consistent with the formation of a stable complex between three glutathione molecules per A

46 inhibition occurs involves the formation of stable complexes between PZP and monomeric Abeta or smal

47 This suggests impaired ability to form stable complexes between the adaptor protein ankyrin R a

48 E2F1 and CDKN1C are found to form stable complexes both in vivo and in vitro.

49 It has been shown, however, that less stable complexes can exchange peptides in the Trans Golg

50 The calculations revealed multiple stable, complex conformations and changes in p38alpha an

51 owever, UL88 does not appear to be part of a stable complex consisting of UL47 and UL48.

52 Together, our study reveals that a stable complex containing MERIT40 acts early in DNA dama

53 -trivial nature of thermal fluctuations when stable complex convective structures emerge.

54 del of the polymerase holoenzyme acting as a stable complex coordinating the replisome, these observa

55 ility of the residual interactions to form a stable complex decreases in an exponential fashion.

56 We hypothesised that more highly stable complexes, delivered using liposomes, may provide

57 ibits homotypic interactions, forming highly stable complexes dependent upon hydrophobic interactions

58 ent DNA cleavage, still allow formation of a stable complex (dissociation rate <0.006 s(-1)), suggest

59 es 92% identity with proCELA3B, did not form stable complexes due to the evolutionary replacement of

60 ind to a P.Z-containing DNA duplex to form a stable complex, effectively mimicking a G.C pair.

61 ion complex (EI) that isomerizes to a highly stable complex (EI*) from which ITMN-191 dissociates ver

62 ferritin and ferritoid are coassembled into stable complex(es) present in embryonic and adult cornea

63 ulated in endosomes, but its ability to form stable complexes following internalization was reduced,

64 addition, thermodynamic properties indicated stable complex formation but higher propensity of protei

65 ts strongly indicate a lipid requirement for stable complex formation in which the likely oligomeric

66 size exclusion chromatography we demonstrate stable complex formation of TRN-SR2 and RanGTP in soluti

67 nd numerous hydrophobic contacts account for stable complex formation with a buried surface area of 3

68 ays, we show that the C-edge is critical for stable complex formation, betaarr1 recruitment, receptor

69 In contrast to stable complex formation, dynamic association of PBP2 is

70 then stalled to the specific sites to form a stable complex formation.

71 e have used atomic force microscopy to study stable complexes formed between HIV-1 integrase and vira

72 ic acid on alpha- and beta-caseins with more stable complexes formed with alpha-casein.

73 higher than that for dissociation (d) of the stable complex ( [Formula: see text] KJ mol(-1)), and th

74 PhoA regions engaged by TF increase, a more stable complex gradually emerges.

75 ata on how these proteins assemble to form a stable complex have not been reported.

76 These remarkably stable complexes have supramolecular structures for enzy

77 an overexpress and purify LptD and LptE as a stable complex in a 1:1 stoichiometry.

78 SFMBT1, LSD1, and CoREST also form a stable complex in germ cells, and their chromatin bindin

79 AGR2 formed a stable complex in human cell lysates with Reptin, thus v

80 analyses, we demonstrate the formation of a stable complex in solution, in which one molecule of the

81 hat these fragments form a high affinity and stable complex in solution.

82 of TbCentrin3 and TbIAD5-1 for maintaining a stable complex in the flagellar axoneme.

83 We showed that SWI5 and MEI5 form a stable complex in vitro and in vivo.

84 idoreductase 1 (Ndor1) and anamorsin--form a stable complex in vivo that was proposed to provide elec

85 directly with Yap1 and these proteins form a stable complex in vivo.

86 owed by unrestrained MD simulations led to a stable complex in which MTERF1 was observed to undergo s

87 latively immobile, suggesting that Gag forms stable complexes in association with YB-1.

88 We show that SmgGDS-607 forms more stable complexes in cells with nonprenylated GTPases tha

89 ated that SNAP23 and ATG16L1 proteins form a stable complex independent of nutrient condition, wherea

90 ever, under 420 nm light irradiation, a more stable complex is again formed between alpha-CD and tran

91 If and how this abundant and normally stable complex is degraded by cells is largely unknown.

92 esults provide strong evidence that the most stable complex is formed between XRCC1 and Polbeta.

93 ations, and form multivalent and kinetically stable complexes is demonstrated as a powerful tool for

94 "kinetic trap" associated with particularly stable complexes is shown to be unlikely because of unfa

95 The calculations find that the most stable complex isolated in room-temperature experiments

96 present in the form of low-molecular weight stable complexes known for their bio-availability.

97 egrase (IN) assembled on viral DNA ends in a stable complex, known as the intasome.

98 le DNA replication, multiple proteins form a stable complex, known as the replisome, enabling them to

99 propose a modified barrier model, in which a stable complex located at the NDR acts as a bidirectiona

100 The most stable complexes (log Kd up to 8.2) were found in the ca

101 mes to regulate meiotic recombination, and a stable complex may be required for sister-chromatid cohe

102 The association of PaaF and PaaG into a stable complex might serve to speed up the steps of the

103 Mre11 and Rad50 form a stable complex (MR) and work cooperatively in repairing

104 HPS1 and HPS4 form a stable complex named biogenesis of lysosome-related orga

105 d into the larger and thermodynamically more stable complex [NH(4)(+)C o-Me(2)-2.2.1], even though th

106 mplex formation from the dissociation of the stable complex occurred in a single step with the activa

107 ation and mass spectroscopy, we identified a stable complex of 174 proteins that were associated with

108 er, and at least a single zipcode to yield a stable complex of [Myo4pShe3pShe2pzipcode] in 2:4:4:1 st

109 This leads to formation of a relatively stable complex of Cosmc and denatured T-synthase accompa

110 Additionally, a stable complex of MRPP1 and MRPP2 has m(1)R9 methyltrans

111 Here we identified a minimal stable complex of murine Rab33B(30-202) Q92L and Atg16L1

112 The absence of ORC1 revealed a compact, stable complex of ORC2-5.

113 We have cocrystallized a stable complex of recombinant N- and C-terminal fragment

114 18-crown-6 in the Cp'3Ln/K reaction, a more stable complex of Tb(2+) was produced as well as more st

115 We successfully identified stable complexes of crenezumab with Abeta pentamer (olig

116 It is the only ligand that supports stable complexes of Mn(3+) and Mn(2+) in biological mili

117 ll characterization of a series of thermally stable complexes of the general formula [Tp'(CO)(2)MSiC(

118 n that the formation of abnormally large and stable complexes of these dynamin mutants in vivo contri

119 ve and translesion polymerases do not form a stable complex on one clamp but alternate their binding.

120 ologically, the ability of RT to form a more stable complex on RNA-DNA may aid in degradation of RNA

121 ping strategy for creating a wide variety of stable complex origami and kirigami structures autonomou

122 y stabilized before the formation of a fully stable complex over approximately 2-3 minutes.

123 ing enzymes of this pathway and show another stable complex, PaaFG, an enoyl-CoA hydratase and enoyl-

124 The air-stable complex Pd(eta(3)-allyl)(DTBNpP)Cl (DTBNpP = di(t

125 The air stable complex [(PNP)FeCl(2)] (1) (PNP = N[2-P(CHMe(2))(

126 The stable complex predominated over free molecules (DeltaG(

127 4), which interact with each other to form a stable complex (PTB1:34).

128 This thermally stable complex quickly evolves chlorine upon irradiation

129 Formation of stable complexes, resistant to high salt, requires ATP h

130 heptanedionate) ligand led to hydrolytically stable complex salts of type [(eta(6)-p-cymene)Ru(beta-d

131 of simulated system complexity, the largest stable complex systems would be unstable if not for vari

132 -complementary oligomers generally form more stable complexes than mismatched duplexes.

133 Archaeal Spt4 and Spt5 form a stable complex that associates with RNAP independently o

134 In vitro, the sole stable complex that contains both meiosis-specific septi

135 lyses, we report that GAPDH and NAMPT form a stable complex that is essential for nuclear translocati

136 with bound nucleotide, forming a remarkably stable complex that is highly resistant to both thapsiga

137 (IV)NC1 binds the CBD of MMP-2 and forming a stable complex that prevents activation of MMP-2.

138 mSNAP190, DmSNAP50 and DmSNAP43) that form a stable complex that recognizes an snRNA gene promoter el

139 al transcription factors and Pol II can form stable complexes that are precursors for functional tran

140 n binding pathways is derived from extremely stable complexes that interact very tightly, with lifeti

141 For each imine, there is a set of stable complexes that represent minima on the potential

142 t this RD-DBD interface is necessary to form stable complexes that support gene expression.

143 ass spectrometry experiments identified four stable complexes: the acyl-carrier proteins ApeE and Ape

144 d unbinding events, but together they form a stable complex through polyvalency.

145 state has high affinity for Cdc37 and forms stable complexes through a multidomain cochaperone inter

146 ydrogen-bond acceptors (e.g., DMPU) can form stable complexes through hydrogen bonding.

147 FA-associated protein 24 kDa (FAAP24) form a stable complex to anchor the FA core complex to chromati

148 estabilized, aggregation-prone proteins in a stable complex under conditions where ER chaperoning cap

149 plete T20 binding site would contribute to a stable complex, which could help to explain why prior st

150 These proteins directly interact and form a stable complex, which has been proposed to accelerate th

151 53BP1 and TIRR form a stable complex, which is required for their expression.

152 MSH2-MSH6 and NHP6A form a stable complex, which is responsive to ATP on mismatched

153 formed ligand/receptor clusters that formed stable complexes, which resisted dissociation by c-kit b

154 mical analyses revealed that the RQC forms a stable complex with 60S ribosomal subunits containing st

155 activates the NF-kappaB pathway by forming a stable complex with a central region (amino acids 150-27

156 vitro, (35)S-SmSrpQ was able to form an SDS-stable complex with a component of the larval lysate, bu

157 f the subunits of dimeric FN, resulting in a stable complex with a slow koff.

158 n the absence of other factors, DOT1 forms a stable complex with AF9 and does not interact with AF9*A

159 GSK3 forms a stable complex with AMPK through interactions with the A

160 SSS may in fact be direct, since SSS forms a stable complex with and antagonizes nAChR function in tr

161 -ETO's DNA-binding domain (AML1-175) forms a stable complex with apo-TRiC.

162 hly dynamic in isolation but together form a stable complex with approximately 100-nM affinity.

163 igmentosa, causes toxicity through forming a stable complex with ARR1.

164 FUS, mutant FUS-R521C proteins formed a more stable complex with Bdnf RNA in electrophoretic mobility

165 of NTSR1 is critical for the formation of a stable complex with betaarr1(DeltaCT), and identify phos

166 ely to interact with the R2 domain to form a stable complex with better alignment in the turn region

167 s suggest that Trm112 is not maintained in a stable complex with Bud23.

168 C5 to generate metastable C5b, which forms a stable complex with C6, termed C5b-6.

169 2, the dominant protein in aCASCADE, forms a stable complex with Cas5a.

170 we purified SCML2B and found that it forms a stable complex with CDK/CYCLIN/p21 and p27, enhancing th

171 nts of ChlB with Strep-ChlN suggested that a stable complex with ChlN is greatly impaired in the subs

172 how that PML isoform II specifically forms a stable complex with CIITA at PML bodies.

173 us effect on in vivo function, even though a stable complex with circular DNA was still observed.

174 Unlike CsoR, CstR does not form a stable complex with Cu(I); operator binding is instead i

175 The pyridinium salt 4H(+) forms a stable complex with cucurbit[7]uril (CB[7]) with 1:1 sto

176 d CRTAP have previously been shown to form a stable complex with cyclophilin B, and P3H1 was shown to

177 ein is a 140-amino acid protein that forms a stable complex with DAT and is linked to the pathogenesi

178 xpressed in dopaminergic neurons and forms a stable complex with DAT in vivo via GST pulldown and co-

179 in the presence of thioredoxin by forming a stable complex with DNA that prevents replication.

180 idues in the HG chain are required to form a stable complex with endogenous HG through calcium comple

181 In the stabilization phase, cofilin formed a stable complex with F-actin, was persistently retained a

182 It formed a highly stable complex with gp41 N-terminal heptad repeat peptid

183 single-ring GroEL variant GroEL(SR) forms a stable complex with GroES, arresting the chaperoning rea

184 Whereas FKBP4 and p23 form a stable complex with hAgo2, the function of Cdc37 in RNAi

185 was defective in heme transfer yet formed a stable complex with Hb (Kd = 6 +/- 2 mum) in solution wi

186 Our results revealed that Red1 forms a stable complex with Hop1 in vitro and provided quantitat

187 In vitro, depolymerized clathrin forms a stable complex with Hsc70*ADP.

188 2 residues of HsiC1 are sufficient to form a stable complex with HsiB1, but the C terminus of HsiC1 i

189 that are paralogous to IDN2 and that form a stable complex with IDN2 in vivo.

190 kinase (or kinase complex), but none form a stable complex with IKKgamma.

191 pproaches, we demonstrate that RGS14 forms a stable complex with inactive Galphai1-GDP at the plasma

192 IntS11 forms a stable complex with Integrator complex subunit 9 (IntS9)

193 Unlike with the azoles, CYP121 forms a stable complex with its natural substrate cYY that does

194 mentation studies showed that c-Abl formed a stable complex with Jak2 in live cells.

195 e, which forms a approximately 60 times more stable complex with K(+) than with NH(4)(+), as confirme

196 g spermatogenesis through the formation of a stable complex with LSD1 and CoREST.

197 s-172 ubiquitination enables RIG-I to form a stable complex with MAVS, thereby inducing IFN signal tr

198 Our study reveals that RPL11 forms a stable complex with MDM2 in vitro through direct contact

199 d protein) oncogene has been found to form a stable complex with members of the Angiomotin (Amot) fam

200 mbinant Drp1 mutants lacking insert B form a stable complex with Mff.

201 rane helix with MraY demonstrating E forms a stable complex with MraY.

202 Rtt109 and Vps75 form a stable complex with nanomolar binding affinity (K(d) = 1

203 sGC forms a stable complex with NO and carbon monoxide (CO), but not

204 or each monomer of the dimeric GPCR within a stable complex with nucleotide-free Gt.

205 lly modified cyclodextrin which gives a more stable complex with OTA than the previously published de

206 rom Drosophila, Gyc-88E, was shown to form a stable complex with oxygen.

207 His-p23 also formed a stable complex with p24, a Wip1 protein of unknown funct

208 but not Delta160p53beta dimer, could form a stable complex with p53-specific DNA, which is consisten

209 We show that CSB forms a stable complex with Pol II and acts as an ATP-dependent

210 ssociation inhibitor (RhoGDI), which forms a stable complex with prenylated Rho GTPases.

211 h liposomes containing VAMP4, resulting in a stable complex with properties resembling canonical SNAR

212 he GDP-bound mutant, is capable of forming a stable complex with R*.

213 RanBP1 can also form a stable complex with Ran and RCC1, although the dynamics

214 for SUMO1 as RanGAP1-SUMO1/UBC9 forms a more stable complex with RanBP2 compared with RanGAP1-SUMO2 t

215 at elevated CYCD3;1 levels, E2FA maintains a stable complex with RBR1 in proliferating cells.

216 is a monomeric and rigid domain that forms a stable complex with reduced TRX1 with 1:1 molar stoichio

217 ring entry, and incoming HPV proteins form a stable complex with retromer subunits.

218 GcrA forms a stable complex with RNA polymerase and localizes to almo

219 or RprA or ArcZ to act in vivo and to form a stable complex with rpoS mRNA in vitro; both were partia

220 We found that Op-IAP3 forms a stable complex with SfIAP, the native, short-lived IAP o

221 egulation of PSPC1, which replaced NONO in a stable complex with SFPQ.

222 The cholesteryl peptides form stable complex with siRNA and effectively protect siRNA

223 Translocated SifA formed a stable complex with SKIP and Rab9 in infected cells.

224 t Las17 is part of a large and biochemically stable complex with Sla1, a clathrin adaptor that inhibi

225 Biochemically, VAMP4 forms a stable complex with SNAREs syntaxin-1 and SNAP-25 that d

226 only the sigma(K) part was needed to form a stable complex with SpoIVFB in a pulldown assay.

227 hat catalyzes E3 ligase activity and forms a stable complex with SUMO-modified RanGAP1 and UBC9 at th

228 se and rat cDNA, we show that CNIH-3 forms a stable complex with tetrameric AMPARs and contributes to

229 ent evidence that the degradosome can form a stable complex with the 70S ribosome and polysomes, and

230 APTES formed a stable complex with the capture antibody that was in tur

231 e results suggested that CENP-B forms a more stable complex with the CENP-A nucleosome through specif

232 Specifically, CENP-B forms a stable complex with the CENP-A nucleosome, when the CENP

233 general transcription factor Bdp1 to form a stable complex with the DNA.

234 The product of gene 5.5 (gp5.5) forms a stable complex with the Escherichia coli histone-like pr

235 meric transmembrane protein that exists in a stable complex with the platelet-derived growth factor (

236 They transformed cells by forming a stable complex with the platelet-derived growth factor b

237 ts with hPCL3 and its paralog PHF1 to form a stable complex with the PRC2 members EZH2, EED, and Suz1

238 n that allows CaMKII and Epac to remain in a stable complex with the receptor.

239 ies its presence in the nucleus by forming a stable complex with the SR protein substrate and appropr

240 P2 promoter, but not the P1 promoter, form a stable complex with two regions of RNAIII near the 5' an

241 ecently, it has been shown that BAG6 forms a stable complex with UBL4A and GET4 and functions in memb

242 zes both the UBA2 and XPCB domains to form a stable complex with Vpr, linking Vpr directly to cellula

243 , we found that mutant FUS proteins formed a stable complex with WT FUS proteins and interfered with

244 It forms a stable complex with XPC in the nucleoplasm under steady-

245 urther revealed that the secreted NA forms a stable complex with Zn(II).

246 D1 retained a high affinity for, and forms a stable complex with, the hydroxylated RPS23 substrate.

247 wild type and mutant Ca(2+)-ATPases to form stable complexes with aluminum fluoride (E2.AlF) and ber

248 ial because they neither colocalize nor form stable complexes with Bax.

249 While aldotetroses form extremely stable complexes with borate, they are not accessible by

250 plice variants have reduced capacity to form stable complexes with COI1 in the presence of the bioact

251 are superior organometallic ligands and form stable complexes with copper(III), silver(III), gold(III

252 e results suggest that (i) DNA can form very stable complexes with counterions, (ii) these complexes

253 Most of these ligands formed stable complexes with CYP121, and their binding did not

254 ficity, as demonstrated by stronger and more stable complexes with deaminase specific ssDNA than with

255 ynamic nonspecific binding to DNA, Fis forms stable complexes with DNA segments that share little seq

256 The H(3)DFOSq ligand can be used to form stable complexes with either of the positron-emitting ra

257 The pliG promoter forms stable complexes with either one or two Zur dimers with

258 enerated MHC class II molecules from forming stable complexes with endogenous self-peptides.

259 Here, we identify PP5 in stable complexes with extracellular signal-regulated kin

260 s of protocatechuic ligand, which could form stable complexes with ferric ions to prevent their preci

261 ctopically expressed PAR1 and PAR2 both form stable complexes with G alpha(q), G alpha(11), G alpha(1

262 Galpha(q)QL and Galpha(13)QL variants formed stable complexes with Gbetagamma, impairing its interact

263 The DPT forms stable complexes with GFX and enhances its solubility, p

264 Empty MHCII molecules form stable complexes with HLA-DM, which are disrupted by bin

265 Pgp3 bound to and formed stable complexes with LL-37.

266 methylation by this bacterium such that less stable complexes with mixed ligation involving LMM-RSH,

267 ility to bind to DMC1 and DNA but forms less stable complexes with MND1 and fails to efficiently stim

268 cipitation experiments showed that NET forms stable complexes with NK1R.

269 nstrate that purified Reptin and Pontin form stable complexes with nucleosomes.

270 al sites that bind NO and CO but do not form stable complexes with O(2).

271 Enterobacterial MlaA proteins form stable complexes with OmpF/C (5,6) , but the porins do n

272 Negatively charged DNA can form extremely stable complexes with positively charged ions.

273 confirmed that PYL4(A194T) was able to form stable complexes with PP2CA in the absence of ABA, in co

274 Both PKGIalpha and PKGIbeta formed detergent-stable complexes with SERT, and this association did not

275 sleep to qvr/sss mutants, and lynx1 can form stable complexes with Shaker-type channels and nAChRs.

276 nd showed that these wild type peptides form stable complexes with six common MHC-II alleles, represe

277 These proteins form stable complexes with SPT.

278 brium binding studies show that POLRMT forms stable complexes with TFB2M or TFAM on LSP with low-nano

279 cytochemistry indicated that Na(v)1.7 formed stable complexes with the beta(1)-beta(3) subunits in vi

280 Translocators were purified as stable complexes with the cognate chaperone PcrH and iso

281 ollective of structured small RNAs that form stable complexes with the conserved protein ProQ.

282 o be potent CARM1 inhibitors and also formed stable complexes with the enzyme.

283 in upstream open reading frames, which form stable complexes with the main, canonical protein encode

284 tic activation of FhCL1 and FhCL2 and formed stable complexes with the mature enzymes.

285 Moreover, only dimeric MxA was able to form stable complexes with the nucleoprotein (NP) of IAV.

286 On tRNA genes, TFIIIB and TFIIIC form stable complexes with the same distinctive occupancy pat

287 nomers derivatized with substituents forming stable complexes with the templates are used.

288 We show that these Est3 homologues form stable complexes with the TEN domain of telomerase rever

289 The receptor forms stable complexes with the test cesium salts, CsCl and Cs

290 lphaB-crystallin oligomers formed long-lived stable complexes with their gammaD-crystallin substrates

291 S365L did not form stable complexes with thrombin or factor Xa, and the I20

292 Sulfoxides are capable of forming stable complexes with transition metals and there have b

293 and tubulin tyrosine ligase (TTL) each form stable complexes with tubulin and inhibit tubulin polyme

294 esent in late endosomes and lysosomes formed stable complexes with type 2 ryanodine receptors (RyR2)

295 ivities, which could explain why UvrA2 forms stable complexes with UvrB on damaged DNA compared with

296 family of molecular containers, able to form stable complexes with various guests, including drug mol

297 show that labile S4 complexes rearrange into stable complexes within a few minutes at 42 degrees C, w

298 showed that 3G11 forms a stoichiometric and stable complex without inducing a significant conformati

299 tide/siRNA complexes, we were able to obtain stable complexes without compromising the helical second

300 er than attack on the thermodynamically more stable complex, yet the major enantiomer of the catalyti