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1 ing the spontaneously generated R* state by "conformational, selection".
2 activated DNA binding by HpNikR is driven by conformational selection.
3 ts indicate that the binding mechanism obeys conformational selection.
4  might be involved in target binding through conformational selection.
5 conservation of symmetry and ligand-directed conformational selection.
6 e in the increased activity of Cel7A through conformational selection.
7 t is whether the mechanism is induced fit or conformational selection.
8 ree enzyme and likely involve some degree of conformational selection.
9 ion including lock-and-key, induced-fit, and conformational selection.
10 eaction, precluding rate enhancement through conformational selection.
11 a previously unseen cooperative mechanism by conformational selection.
12 asing substrate concentration, a hallmark of conformational selection.
13 1(-) CBr(4) CM-1(-) pathway corresponding to conformational selection.
14 uch opposite patterns are also diagnostic of conformational selection.
15 ligand binding according to the mechanism of conformational selection.
16 , P450 17A1 binds its steroid substrates via conformational selection.
17 which the ligand selects the optimal fit via conformational selection.
18  relaxation, a key distinguishing feature of conformational selection.
19 g of [Formula: see text] that occurs through conformational selection.
20 ally distinct topologies that may facilitate conformational selection.
21 ensemble and thus fine-tune activity through conformational selection.
22 en two classical mechanisms: induced-fit and conformational selection.
23 ds first and then assembles with the core by conformational selection.
24 /TM6 hole is apparently not involved in this conformational selection.
25 e opportunities and limitations of design by conformational selection.
26 ed-fit and of specific hydrogen bonds during conformational selection.
27 target via an induced-fit pathway instead of conformational selection.
28 esults from a combination of induced fit and conformational selection.
29 ired for polypyrimidine-tract recognition by conformational selection.
30 discordance in the parameters, indicative of conformational-selection.
31  multiple ligand occupancy, induced-fit, and conformational-selection.
32 s ligand rolapitant in a mechanism involving conformational-selection.
33       Zymogen autoactivation is explained by conformational selection, a basic property of the trypsi
34 lded OMPs to chaperones and, by facilitating conformational selection after release from chaperones,
35 gand gating, cooperativity, induced fit, and conformational selection all from the same set of MISC d
36  earlier studies have also found cases where conformational selection alone could not adequately expl
37 the preservation of antibody binding through conformational selection, altered ACE2 recognition and i
38 be targeted by small ligands always includes conformational selection, although other recognition mec
39 , stabilizing conformational changes through conformational selection and frequently modulates local
40  TCR binding, incorporating elements of both conformational selection and induced fit in a manner tha
41                                    With both conformational selection and induced fit models consider
42 s that underpin DA systems, which fall under conformational selection and induced fit models, and whi
43 ingle-molecule FRET experiments suggest that conformational selection and induced fit of the U2AF(65)
44                            We find that both conformational selection and induced fit play a role in
45       These studies support a model in which conformational selection and induced fit play important
46  competing mechanisms of ligand recognition, conformational selection and induced fit, have dominated
47 nition in solution involves a combination of conformational selection and induced fit, rather than bi
48 elative tendencies to fold via mechanisms of conformational selection and induced fit, respectively.
49 ings illustrate the subtle interplay between conformational selection and induced fit.
50 that binding occurs through a combination of conformational selection and induced-fit mechanisms that
51  kinetic measurements to distinguish between conformational selection and induced-fit models.
52 ts suggest that ADP binding to F1 occurs via conformational selection and is preceded by the transiti
53                                       Mutual conformational selection and population shift followed b
54                            According to the "conformational selection and population shift" theory, l
55 data showed that the interaction occurred by conformational selection and the peptide acquired simila
56 the smFRET distributions are consistent with conformational selection and with inter-state exchange l
57 g, are strong determinants of the mechanism (conformational selection and/or induced fit) of molecula
58  ligand and receptor structural elements for conformational selection, and support co-evolution of Gn
59 6, 3A4, 4A11, and 21A2 was best described by conformational-selection, and P450 2E1 appeared to fit e
60  Our data provide strong evidence supporting conformational selection as a major mechanism for substr
61  Our results highlight both local and global conformational selection as a means for universal 3' spl
62                             We conclude that conformational selection as a mechanism for a ligand bin
63 study emphasizes the preexisting equilibrium/conformational selection as a mechanism for protein-prot
64 d the phosphoprotein Dishevelled, supporting conformational selection as a prerequisite for functiona
65        CypA interacts with its substrate via conformational selection as the configurations of the su
66                    This observation suggests conformational selection as the general mechanism of all
67                       These results identify conformational selection as the mechanism for inhibiting
68 450 4A11 bound the substrate lauric acid via conformational-selection, as did P450 2C8 with palmitic
69                              We propose that conformational selection at microtubule ends favors long
70 nsitive to their chemical environments, with conformational selection available as an evolved mechani
71 establish that dark reversion is governed by conformational selection between two substates, whereby
72                Constrained by the disulfide, conformational selection between weak and tight binding
73                         These data suggest a conformational selection binding mechanism in which the
74 lical conformations, possibly facilitating a conformational selection binding mechanism.
75 nded FKBP51 domain is more consistent with a conformational selection binding process.
76 n k(obs) with [L] is unequivocal evidence of conformational selection, but an increase in k(obs) with
77 r-CBD interface is dispensable for intra-CBD conformational selection, but is indispensable for full
78 ptor activation involves ligand induction or conformational selection, but the molecular basis of the
79                                              Conformational selection by small molecules expands inhi
80 0 muM Mg(2+) generally shifts docking toward conformational selection by stabilizing a folded-like co
81  "induced fit" mechanism (binding first) or "conformational selection" (conformational change first).
82  is populated to only ~1.3%, indicating that conformational selection contributes negligibly to the c
83  is only accessible to Abl and not to c-Src (conformational selection control).
84 ing point in the mechanism is established by conformational selection, controlled by the interaction
85 ng conditions, folding was found to follow a conformational selection (CS) mechanism.
86 o shed light on the long debate over whether conformational selection (CS) or induced fit (IF) is the
87  that include protein conformational change, conformational selection (CS) or induced fit (IF), best
88 ompetent conformations to which ligands bind conformational selection (CS) or whether ligands induce
89  molecular recognition, induced fit (IF) and conformational selection (CS), play a central role in al
90 anism of binding obeying induced fit (IF) or conformational selection (CS).
91  biomolecular switches: induced fit (IF) and conformational selection (CS).
92        In summary, our results indicate that conformational selection dictates stable retinal binding
93 nding protein (ChoX) to be approximately 90% conformational selection dominant under experimental con
94 loosely coupled to the ATPase reaction, with conformational selection driving the motor mechanism.
95 rbations is reminiscent of binding events by conformational selection encountered in other riboswitch
96 ore enables 627-NLS to bind importin through conformational selection from a temperature-dependent eq
97                        Our data suggest that conformational selection guides beta-arrestin recruitmen
98  Discussion concerning "induced fit" versus "conformational selection" has, however, ignored detoxica
99  Na(+) binding and functional selectivity by conformational selection (i.e., preference of the allost
100 like configurations--that implies a role for conformational selection in ligand binding.
101  and active site dynamics, with evidence for conformational selection in the kinase core of 2P-ERK2 b
102 bstrate access, which extends the concept of conformational selection in trypsin-related proteases.
103 tems agree with our recently proposed hybrid conformational selection/induced-fit models.
104                                              Conformational selection is an established mechanism in
105                  It has been speculated that conformational selection is an integral component of sub
106                            Here we show that conformational selection is associated with a rich reper
107 ins bind their substrates via induced fit or conformational selection is not understood.
108         A reaction-controlled model invoking conformational selection is proposed to explain the slow
109 f human P450-substrate interactions and that conformational-selection is a dominant feature of many o
110 ton follows a combination of induced-fit and conformational-selection-like mechanisms, via partial bi
111 onformational changes, i.e."induced fit" or "conformational selection," mainly determined by the inte
112 r dynamics-generated ensembles suggests that conformational selection may play a hitherto unappreciat
113 host and provides the first observation of a conformational selection mechanism (as opposed to induce
114    The latter is shown to be controlled by a conformational selection mechanism and also by differenc
115 tion that facilitates drug binding through a conformational selection mechanism and increases the bin
116              Pyrophosphorolysis occurs via a conformational selection mechanism as the pyrophosphate
117                                         This conformational selection mechanism contrasts with the lo
118 here indicate that the RNA aptamer employs a conformational selection mechanism for binding theophyll
119 osed" and "open" conformations, suggesting a conformational selection mechanism for pilus binding.
120                                This favors a conformational selection mechanism for release of the fi
121 librium dynamics within the domain suggest a conformational selection mechanism in the rapid associat
122 esults provide strong evidence that VcINDY's conformational selection mechanism is a result of the so
123                                            A conformational selection mechanism is proposed to accoun
124 , suggesting that either an induced fit or a conformational selection mechanism should contribute to
125 hese findings can be explained in light of a conformational selection mechanism that dictates that co
126  are also affected by calreticulin through a conformational selection mechanism that facilitates MHC-
127 se, beta-rich conformers self-assemble via a conformational selection mechanism to form energetically
128  Ly49H/m157 and Ly49I/m157 interactions is a conformational selection mechanism where only the extend
129 ation through a significant component of the conformational selection mechanism, because they may inc
130 c and computational studies that show that a conformational selection mechanism, in which POT1 bindin
131 related with ligand efficacies, supporting a conformational selection mechanism.
132 transition pathway, thus precluding a simple conformational selection mechanism.
133 unknown, and activation proceeds through the conformational selection mechanism.
134 and suggest that glucagon binds to GCGR by a conformational selection mechanism.
135  which seems to be in contradiction with the conformational selection mechanism.
136  selects the most complementary one, via the conformational selection mechanism?
137 hat binding specificity was controlled by a "conformational selection" mechanism.
138 ng scenarios with the potential to show that conformational selection might be the design principle o
139                   The data support a passive conformational selection model by which the protein sele
140 ide direct structural evidence in favor of a conformational selection model for basal activity in bet
141 slational T-box riboswitches; and supports a conformational selection model for NCCA recognition.
142 sic flexibility of proteins, which follows a conformational selection model for protein-protein inter
143 ur comparative NMR analyses lead to a double conformational selection model in which each apo CBD dyn
144 on, the structural data demonstrate that the conformational selection model is not sufficient to expl
145 tion to the WT-like state, consistent with a conformational selection model of ligand binding, but st
146                         This agrees with the conformational selection model of molecular recognition,
147                         On the contrary, the conformational selection model postulates that prion iso
148                             Alternatively, a conformational selection model proposes that a minor pop
149                                          The conformational selection model requires that the protein
150    Based on these findings, we established a conformational selection model that governs substrate bi
151                                            A conformational selection model that includes equilibrium
152                         The proposed inverse conformational selection model will extend also to lipid
153 vel model of protein regulation, the "Double-Conformational Selection Model", which demonstrates how
154                                       In the conformational selection model, a protein samples a scar
155  effect is readily interpreted in terms of a conformational selection model, in which p51(L289K) has
156 hat allostery in TetR is well described by a conformational selection model, in which the apo state s
157 ation is adequately explained by a two-state conformational selection model, the partial agonism of c
158 e catalytic data confirm an extension of the conformational selection model, wherein different substr
159 rst is the induced fit and the second is the conformational selection model.
160 he induced fit model and not required by the conformational selection model.
161  3A4 was consistent with an induced-fit or a conformational-selection model, but the concentration de
162 ne to P450 21A2 was also best described by a conformational-selection model.
163 ccurring after the conformational change via conformational selection of an energetically disfavored
164 model where specificity is generated through conformational selection of an intrinsically bent DNA se
165 ss-seeding of amyloid species is governed by conformational selection of compatible (complementary) s
166                          Nb binding involves conformational selection of LacY molecules with exposed
167 that complex formation may be facilitated by conformational selection of residual structure in the ac
168 and that capsid assembly likely proceeds via conformational selection of sparsely populated configura
169              Moreover, the robustness of the conformational selection of the dynamic ensemble is eval
170     Enzyme kinetics data are consistent with conformational selection of the ensemble of active domai
171 usion-limited k(on) ~ 10(11) M(-1) s(-1) via conformational selection of the wobble conformation, whi
172 ited protein states originate primarily from conformational selections of loops AB and GH, a portal r
173                                  Previously, conformational selections of the AB and GH loops have be
174 o equilibrium, k(obs), becomes diagnostic of conformational selection or induced fit based on whether
175 g to P450 2E1 could be described by either a conformational-selection or an induced-fit model.
176 formational heterogeneity is present before (conformational selection) or after (induced fit) ligand
177                   These studies validate the conformational selection paradigm for the pleiotropic fu
178 chanism switches from being dominated by the conformational selection pathway at low ligand concentra
179 s formed in the rate-limiting step along the conformational selection pathway but after the rate-limi
180 scription of a high-energy enzyme state in a conformational selection pathway by an experimental stra
181      Strikingly, the assembly rate along the conformational selection pathway resembles that of an is
182 find evidence for the existence of canonical conformational selection pathways.
183 rget molecules through either induced fit or conformational selection pathways.
184                                              Conformational selection plays a key role in the polymer
185 equired to form the E-S complex suggest that conformational selection plays a role in substrate recog
186                          The induced fit and conformational selection/population shift models are two
187                 This framework predicts that conformational selection prevails on ubiquitin's paradig
188  to form complexes with G proteins through a conformational selection process.
189 ing may proceed largely through a process of conformational selection rather than induced fit.
190         Binding of Sox2 to DNA thus involves conformational selection, rather than exclusively induce
191 ignaling pathways, which could be related to conformational selection, signaling amplification, and p
192            In the apo protein, an allosteric conformational selection step comprising almost 60% of t
193 ng adrenodoxin results in enhancement of the conformational selection step.
194 closed model containing both induced fit and conformational selection steps.
195 esembled the response of proteins undergoing conformational selection, suggesting an energy landscape
196 nt simulations strongly support an "extended conformational selection" synergistic folding mechanism
197 ation modeling was also more consistent with conformational selection than with an induced-fit mechan
198 d cross-bridges that appear to result from a conformational selection that occurs during the weak bin
199  with the previously suggested role of E3 in conformational selection, the large positive entropy sug
200 rstood and proposed to primarily operate via conformational selection, the mechanism underlying allos
201 nal shift" or "deformed templating" and the "conformational selection." The conformational shift hypo
202 the accuracy of their widths needed to drive conformational selection thereby increasing the experime
203  all three collagen chains and binds through conformational selection to a sequence that is one tripl
204  the binding mechanism gradually shifts from conformational selection to induced fit.
205 t between the two TCRs: whereas A6 relies on conformational selection to select and bind different li
206  Adk suggests a two-step mechanism combining conformational selection to this state, followed by an i
207 ding support for adaptive recognition via a 'conformational selection' type mechanism.
208 imetic camelid antibody fragment isolated by conformational selection using yeast surface display.
209                       Here we show that the "conformational selection versus induced fit" distinction
210 apid kinetics support a binding mechanism of conformational selection where the Na(+)-binding site is
211 anges are realized through the mechanisms of conformational selection (where a higher-energy minimum
212  model of molecular recognition dominated by conformational selection, whereas only minor structural
213 ollows an integrated mechanism that combines conformational selection with induced folding steps.
214 folding, which continues to follow "extended conformational selection" with multiple stages of select
215 ts suggest that glycan recognition occurs by conformational selection within the ground state; this m

 
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