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1 ynthetic enzymes with the cytoskeleton via a stable complex.
2 ging 'dynamic complex' rather than a typical stable complex.
3 native mechanism to facilitate assembly of a stable complex.
4 20 conformation of the glycoprotein led to a stable complex.
5 oE, binding of the protein results in a more stable complex.
6 Tah1 binds to the Pih1 C terminus to form a stable complex.
7 f Tah1 to Pih1 allows for the formation of a stable complex.
8 domain binds preferably Cu(II) ion forming a stable complex.
9 udies clearly reveal that LumC13-ALK5 form a stable complex.
10 s of interaction with heme to form this very stable complex.
11 igand to fold with the binding groove into a stable complex.
12 h cytosolic beta-subunits (Kvbeta) to form a stable complex.
13 n between these sites are required to form a stable complex.
14 s and physically interact as a biochemically stable complex.
15 ratio is important to produce a soluble and stable complex.
16 idual gammaTuSC components for maintaining a stable complex.
17 ric-field-induced slow dissociation of these stable complexes.
18 ty, 4oo, produces the most thermodynamically stable complexes.
19 dissociation rates, indicating formation of stable complexes.
20 ediates that subsequently relax to specific, stable complexes.
21 bation leading to an increased population of stable complexes.
22 sphine 1 with K(2)PtCl(4) afforded the bench stable complex 3 which upon treatment with Ag[CB(11)H(6)
23 plekin, CPSF73, and CPSF100 are present in a stable complex and interact with histone-specific proces
24 es demonstrated that KLF15 and the GR form a stable complex and that these stress-induced transcripti
26 o encourage more studies on the dynamics of "stable" complexes and to provide a word of caution about
27 ly interacts with Hha (rather than forming a stable complex) and enhances the spontaneous oxidation o
28 We find the CH3 homodimer to be a highly stable complex, and its dissociation force of >150 pN at
30 sulted in shortened M-C bond lengths for the stable complexes, and it was found that Fe(nor)4 receive
31 nvestigations were performed to test whether stable complexes are formed by additional selected TGF-b
33 he amino-terminal sensor domain is to form a stable complex as a functional kinase, but possibly not
34 e short, conserved promoter sequences form a stable complex at physiological temperatures, and this c
35 e slightly longer Ku-(1-253) homodimer forms stable complexes at both ends of linear plasmid DNA that
37 sipation (QCM-D) resolved the formation of a stable complex between CymA and one of its native redox
38 rogen transcription factor TnrA by forming a stable complex between FBI-GS and TnrA that inhibits Tnr
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
42 inhibitors of alpha-syn aggregation, but no stable complex between the sHsps and alpha-syn was detec
44 which is consistent with the formation of a stable complex between three glutathione molecules per A
46 the Saccharomyces cerevisiae ORC that form a stable complex bind to origins of DNA replication and re
48 thanide complexes have been synthesized from stable complexes by diazotization and azo-compound forma
53 ibits homotypic interactions, forming highly stable complexes dependent upon hydrophobic interactions
54 ent DNA cleavage, still allow formation of a stable complex (dissociation rate <0.006 s(-1)), suggest
55 es 92% identity with proCELA3B, did not form stable complexes due to the evolutionary replacement of
56 ion complex (EI) that isomerizes to a highly stable complex (EI*) from which ITMN-191 dissociates ver
57 ferritin and ferritoid are coassembled into stable complex(es) present in embryonic and adult cornea
58 PNP), a nonhydrolyzable ATP analog, promotes stable complex formation between RecQ4 and single-strand
59 ts strongly indicate a lipid requirement for stable complex formation in which the likely oligomeric
60 size exclusion chromatography we demonstrate stable complex formation of TRN-SR2 and RanGTP in soluti
61 nd numerous hydrophobic contacts account for stable complex formation with a buried surface area of 3
65 e have used atomic force microscopy to study stable complexes formed between HIV-1 integrase and vira
73 analyses, we demonstrate the formation of a stable complex in solution, in which one molecule of the
78 idoreductase 1 (Ndor1) and anamorsin--form a stable complex in vivo that was proposed to provide elec
79 man ISD11 and shown that human ISD11 forms a stable complex in vivo with the human cysteine desulfura
81 owed by unrestrained MD simulations led to a stable complex in which MTERF1 was observed to undergo s
84 We also determined that DIM-2 and HP1 form a stable complex independently of the trimethylation of hi
88 ations, and form multivalent and kinetically stable complexes is demonstrated as a powerful tool for
89 "kinetic trap" associated with particularly stable complexes is shown to be unlikely because of unfa
92 le DNA replication, multiple proteins form a stable complex, known as the replisome, enabling them to
93 propose a modified barrier model, in which a stable complex located at the NDR acts as a bidirectiona
95 mes to regulate meiotic recombination, and a stable complex may be required for sister-chromatid cohe
99 ation and mass spectroscopy, we identified a stable complex of 174 proteins that were associated with
100 er, and at least a single zipcode to yield a stable complex of [Myo4pShe3pShe2pzipcode] in 2:4:4:1 st
101 This leads to formation of a relatively stable complex of Cosmc and denatured T-synthase accompa
104 18-crown-6 in the Cp'3Ln/K reaction, a more stable complex of Tb(2+) was produced as well as more st
105 of cyclizing NAD, the crystal structure of a stable complex of the cyclase with an NAD analog, ribosy
108 n that the formation of abnormally large and stable complexes of these dynamin mutants in vivo contri
109 ve and translesion polymerases do not form a stable complex on one clamp but alternate their binding.
110 ologically, the ability of RT to form a more stable complex on RNA-DNA may aid in degradation of RNA
111 ping strategy for creating a wide variety of stable complex origami and kirigami structures autonomou
113 ing enzymes of this pathway and show another stable complex, PaaFG, an enoyl-CoA hydratase and enoyl-
116 Cross-functioning pairs that do not form stable complexes produce less hydrogen peroxide and leak
120 heptanedionate) ligand led to hydrolytically stable complex salts of type [(eta(6)-p-cymene)Ru(beta-d
122 bitors and the fact that CK1 and MDM2 form a stable complex suggest that the MDM2 x CK1 complex is a
127 with bound nucleotide, forming a remarkably stable complex that is highly resistant to both thapsiga
129 y one electron to [Re(DPPBT)(3)](+) yields a stable complex that rapidly and reversibly binds ethylen
130 mSNAP190, DmSNAP50 and DmSNAP43) that form a stable complex that recognizes an snRNA gene promoter el
131 al transcription factors and Pol II can form stable complexes that are precursors for functional tran
132 n binding pathways is derived from extremely stable complexes that interact very tightly, with lifeti
135 state has high affinity for Cdc37 and forms stable complexes through a multidomain cochaperone inter
137 FA-associated protein 24 kDa (FAAP24) form a stable complex to anchor the FA core complex to chromati
139 estabilized, aggregation-prone proteins in a stable complex under conditions where ER chaperoning cap
140 nificantly, Ad5E1A, CtBP1, and ZNF217 form a stable complex which requires CR3 and the PLDLS motif.
141 plete T20 binding site would contribute to a stable complex, which could help to explain why prior st
142 These proteins directly interact and form a stable complex, which has been proposed to accelerate th
145 formed ligand/receptor clusters that formed stable complexes, which resisted dissociation by c-kit b
146 mical analyses revealed that the RQC forms a stable complex with 60S ribosomal subunits containing st
147 activates the NF-kappaB pathway by forming a stable complex with a central region (amino acids 150-27
148 vitro, (35)S-SmSrpQ was able to form an SDS-stable complex with a component of the larval lysate, bu
151 n the absence of other factors, DOT1 forms a stable complex with AF9 and does not interact with AF9*A
153 ne hRPA heterotrimer is sufficient to form a stable complex with an unfolded 26-mer G-quadruplex prio
154 SSS may in fact be direct, since SSS forms a stable complex with and antagonizes nAChR function in tr
158 FUS, mutant FUS-R521C proteins formed a more stable complex with Bdnf RNA in electrophoretic mobility
159 ely to interact with the R2 domain to form a stable complex with better alignment in the turn region
163 gate formation because it forms an extremely stable complex with CB7 (K approximately = 10(12) M(-1))
164 we purified SCML2B and found that it forms a stable complex with CDK/CYCLIN/p21 and p27, enhancing th
165 nts of ChlB with Strep-ChlN suggested that a stable complex with ChlN is greatly impaired in the subs
167 us effect on in vivo function, even though a stable complex with circular DNA was still observed.
170 d CRTAP have previously been shown to form a stable complex with cyclophilin B, and P3H1 was shown to
171 ein is a 140-amino acid protein that forms a stable complex with DAT and is linked to the pathogenesi
172 xpressed in dopaminergic neurons and forms a stable complex with DAT in vivo via GST pulldown and co-
173 idues in the HG chain are required to form a stable complex with endogenous HG through calcium comple
175 In the stabilization phase, cofilin formed a stable complex with F-actin, was persistently retained a
176 ect cells, a small fraction of FANCI forms a stable complex with FANCD2 (Fanconi anemia complementati
177 hat PZ dissociated from ZPI once ZPI forms a stable complex with FXa, and kinetic analyses confirmed
179 single-ring GroEL variant GroEL(SR) forms a stable complex with GroES, arresting the chaperoning rea
181 was defective in heme transfer yet formed a stable complex with Hb (Kd = 6 +/- 2 mum) in solution wi
183 ) compromises the ability of hSUV3 to form a stable complex with hPNPase to degrade dsRNA substrates
185 2 residues of HsiC1 are sufficient to form a stable complex with HsiB1, but the C terminus of HsiC1 i
186 his study, we found that mouse Ahi1 formed a stable complex with huntingtin-associated protein 1 (Hap
189 pproaches, we demonstrate that RGS14 forms a stable complex with inactive Galphai1-GDP at the plasma
193 e, which forms a approximately 60 times more stable complex with K(+) than with NH(4)(+), as confirme
194 y for folding, and forms a thermodynamically stable complex with KIX without compromising binding kin
196 s-172 ubiquitination enables RIG-I to form a stable complex with MAVS, thereby inducing IFN signal tr
198 d protein) oncogene has been found to form a stable complex with members of the Angiomotin (Amot) fam
199 homolog of the ScPSO4/PRP19 (hPso4) forms a stable complex with Metnase on both TIR and non-TIR DNA.
205 lly modified cyclodextrin which gives a more stable complex with OTA than the previously published de
209 h liposomes containing VAMP4, resulting in a stable complex with properties resembling canonical SNAR
212 for SUMO1 as RanGAP1-SUMO1/UBC9 forms a more stable complex with RanBP2 compared with RanGAP1-SUMO2 t
215 is a monomeric and rigid domain that forms a stable complex with reduced TRX1 with 1:1 molar stoichio
218 or RprA or ArcZ to act in vivo and to form a stable complex with rpoS mRNA in vitro; both were partia
223 t Las17 is part of a large and biochemically stable complex with Sla1, a clathrin adaptor that inhibi
226 hat catalyzes E3 ligase activity and forms a stable complex with SUMO-modified RanGAP1 and UBC9 at th
227 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
231 e results suggested that CENP-B forms a more stable complex with the CENP-A nucleosome through specif
233 tition between the N and C termini to form a stable complex with the central hydrophobic cluster.
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 (
237 ts with hPCL3 and its paralog PHF1 to form a stable complex with the PRC2 members EZH2, EED, and Suz1
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
246 D1 retained a high affinity for, and forms a stable complex with, the hydroxylated RPS23 substrate.
248 wild type and mutant Ca(2+)-ATPases to form stable complexes with aluminum fluoride (E2.AlF) and ber
249 of this mutant, Int S12A, E449K, could form stable complexes with attP/attB, attL/attR, attL/attL an
252 plice variants have reduced capacity to form stable complexes with COI1 in the presence of the bioact
253 are superior organometallic ligands and form stable complexes with copper(III), silver(III), gold(III
254 e results suggest that (i) DNA can form very stable complexes with counterions, (ii) these complexes
256 ficity, as demonstrated by stronger and more stable complexes with deaminase specific ssDNA than with
257 ynamic nonspecific binding to DNA, Fis forms stable complexes with DNA segments that share little seq
261 s of protocatechuic ligand, which could form stable complexes with ferric ions to prevent their preci
262 ctopically expressed PAR1 and PAR2 both form stable complexes with G alpha(q), G alpha(11), G alpha(1
269 ility to bind to DMC1 and DNA but forms less stable complexes with MND1 and fails to efficiently stim
275 confirmed that PYL4(A194T) was able to form stable complexes with PP2CA in the absence of ABA, in co
276 Both PKGIalpha and PKGIbeta formed detergent-stable complexes with SERT, and this association did not
277 sleep to qvr/sss mutants, and lynx1 can form stable complexes with Shaker-type channels and nAChRs.
278 nd showed that these wild type peptides form stable complexes with six common MHC-II alleles, represe
279 brium binding studies show that POLRMT forms stable complexes with TFB2M or TFAM on LSP with low-nano
280 cytochemistry indicated that Na(v)1.7 formed stable complexes with the beta(1)-beta(3) subunits in vi
285 Moreover, only dimeric MxA was able to form stable complexes with the nucleoprotein (NP) of IAV.
287 bitory activity toward matriptase, forms SDS-stable complexes with the serine protease, and blocks ma
288 We show that these Est3 homologues form stable complexes with the TEN domain of telomerase rever
290 lphaB-crystallin oligomers formed long-lived stable complexes with their gammaD-crystallin substrates
293 and tubulin tyrosine ligase (TTL) each form stable complexes with tubulin and inhibit tubulin polyme
294 These results establish that MRAP forms stable complexes with two different melanocortin recepto
295 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
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