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1 ficiently cross linked, and myosin has to be processive.
2  phosphorylation is distributive rather than processive.
3  directing substrates to the distributive or processive 3' to 5' exoribonuclease activities of Rrp6 o
4                                Its dominant, processive 5'-3' exonuclease and secondary 5'-flap endon
5 rs based on covalent chemistry and is weakly processive (6 +/- 1 steps per outing).
6 Lin28-stimulated oligo-uridylation, which is processive, a distributive mode is employed by TUT7 for
7                       Myosin Va (myoVa) is a processive, actin-based molecular motor essential for in
8  differences between the in vitro apparently processive activity and in vivo distributive monouridyly
9                                Pauses during processive activity on both types of DNA exhibited ATP d
10 4 (Dis3) and Rrp6 subunits to modulate their processive and distributive 3'-to-5' exoribonuclease act
11 ntains 10 Sec residues (SEPP1) suggests that processive and efficient Sec incorporation occurs in viv
12 almodulin binding protein)) exhibited highly processive and fast motility (up to 0.6 mum s(-1)).
13  model of DNA replication describes a highly-processive and largely continuous process by which the g
14 ay important regulatory roles in this highly processive and ordered process.
15 tion of ParA DNA binding activity to enforce processive and pole-directed centromere segregation, pre
16 assays, we show that Kif18B is only modestly processive and that the motor switches frequently betwee
17   Compared with kinesin-1, kinesin-2 is less processive, and its processivity is more sensitive to lo
18 NA synthesis during HR is conservative, less processive, and more mutagenic than replicative DNA synt
19 d direct interactions of cargo with a highly processive anterograde motor.
20  Our recent studies showed that KIF3AC is as processive as conventional kinesin-1, suggesting that th
21 hyscomitrella patens and found that none are processive as native dimers.
22 ilaments display alternating phases of rapid processive assembly and arrested growth, driven by a "pi
23 ociation with barbed ends, followed by rapid processive assembly and release of Spire.
24 es Spire from the barbed end to elicit rapid processive assembly from profilin.actin.
25 -tail with DADs from other formins tunes the processive association with the barbed end, indicating t
26 PolD2-PolD3) is much more efficient and more processive at bypassing a 1,2-intrastrand d(GpG)-cisplat
27 acer sequences through a mechanism involving processive, ATP-dependent Cas3 translocation along forei
28 eneral design guidelines to construct highly processive, autonomous DNA walker systems and to regulat
29         The Phi29 DNA polymerase (DNAP) is a processive B-family replicative DNAP.
30 ther drops as rebinding increases and pseudo-processive behavior becomes possible.
31 atalyzed by the glycosyltransferase GlfT2, a processive carbohydrate polymerase, which generates a se
32 in-recruited ZAP-70, which suggests a weakly processive catalysis on membranes.
33 nsideration of DNA looping in the context of processive catalysis provides new mechanistic insights a
34 e enzyme on interfaces and should facilitate processive catalysis.
35  which is of interest for the development of processive catalysts, i.e., catalysts that thread onto p
36 cally and industrially important GH Family 7 processive cellulases with free energy perturbation/repl
37                   The molecular mechanism of processive chitin synthesis is not understood, limiting
38   The method was applied to the study of the processive chitinase ChiA from Serratia marcescens.
39                        Blunt termini promote processive cleavage, while 3' overhanging termini are cl
40                    BLM is significantly less processive compared to the highly efficient GQ destabili
41 anslocates by a disaccharide unit during the processive cycle of a glycoside hydrolase family 7 cello
42 ard directions, and also produce the fastest processive cytoskeletal motor measured so far, reaching
43  approximately 800 nt gRNA precursors, their processive degradation to a mature size of 40-60 nt, and
44 ation solubilizes its outer surface allowing processive degradation.
45 d oligomeric proteins that are essential for processive deoxyribonucleic acid replication.
46 from the substrate interface followed by its processive depolymerization to soluble sugars.
47 s provide new insights into the mechanism of processive digestion that will be discussed.
48 igate the movement of fluorescently labeled, processive, dimeric motor proteins and propose a unified
49 ion between the heads, the model still shows processive directional stepping, but it becomes uncoordi
50 sK/SpoIIIE translocases move DNA in a highly processive, directional manner, where directionality is
51 a-SNAP binding events may occur as part of a processive disassembly mechanism.
52 hich makes the RNA-DNA primers accessible to processive DNA pols.
53                                     A highly processive DNA polymerase was conjugated to the nanopore
54 ate region accurately and efficiently during processive DNA repeat synthesis has remained elusive.
55  sliding clamp), is rapidly exchanged during processive DNA replication.
56 e DNA and associate with DNA polymerases for processive DNA replication.
57 o be modified as a consequence of disrupting processive DNA replication.
58 A) adopts a ring-shaped structure to promote processive DNA synthesis, acting as a sliding clamp for
59 le recombinant protein that is functional in processive DNA synthesis.
60  DNAP that can couple strand displacement to processive DNA synthesis.
61 w know that PCNA does much more than promote processive DNA synthesis.
62 e and as an essential component required for processive DNA synthesis.
63                      Hexameric helicases are processive DNA unwinding machines but how they engage wi
64 t of the conserved domains, YonO is a highly processive DNA-dependent RNA polymerase.
65                     We conclude that AdnAB's processive DSB unwinding activity suffices for AdnAB fun
66            These enzyme complexes are highly processive, duplex unwinding and degrading machines that
67 ate, leading to a dramatic increase in fast, processive dynein motility.
68 y and can synergize with dynactin to enhance processive dynein movement.
69 also increases the frequency and velocity of processive dynein movements that are activated by comple
70  offers insight into how cargo adaptors form processive dynein-dynactin motor complexes.
71 py to study the interaction of LIS1 with the processive dynein-dynactin-BicD2N (DDB) complex.
72 in the catalytic cycle based on RNA binding, processive elongation activity, and single nucleotide in
73 al polymerases, was found to be critical for processive elongation and virus growth.
74 ly65Val allele in Li1 plants likely disrupts processive elongation of F-actin, resulting in a disorga
75 eins act as actin polymerases that drive the processive elongation of filament barbed ends in membran
76                                              Processive elongation of RNA Polymerase II from a proxim
77 d subsequent intermediates leading to highly processive elongation, and we examined the effects of fo
78 om preferential substrate binding but during processive elongation.
79 e transition from distributive initiation to processive elongation.
80                   Loop formation followed by processive enlargement provides a mechanism by which con
81  the discovery that the HECT E3 Nedd4-1 is a processive enzyme and that disruption of its processivit
82 ces cerevisiae Pol delta-PCNA is a rapid and processive enzyme, suggesting that CMG may bind and alte
83 from Escherichia coli is a uniquely fast and processive enzyme.
84 terified zones, indicating that it acts as a processive enzyme.
85 CsaB is a distributive enzyme, and CsxA is a processive enzyme.
86  the alginate polymer suggest that AlgG is a processive enzyme.
87                                              Processive enzymes are major components of the efficient
88                                      Whereas processive enzymes bind only once to a substrate before
89 ave indicated that kinesin-14 motors are non-processive enzymes, working in the context of multi-moto
90 leotide precision using nanopores coupled to processive enzymes.
91 dicate that this organization helps to drive processive exo-ribonucleolytic cleavage.
92 le by sequentially measuring the products of processive exopeptidase digestion, or by using a molecul
93                         RNase II, a 3' to 5' processive exoribonuclease, is the major hydrolytic enzy
94 llulose is produced by cellulose synthase, a processive family-2 glycosyltransferase.
95                                Dia is a more processive, faster elongator, paralleling the long, stab
96        This is the direct demonstration of a processive formin from plants.
97 ng cell nuclear antigen and participation in processive genome replication are common features of FAM
98 uggest that B35DNAP may perform faithful and processive genome replication in vivo and, when required
99  heterodimeric co-factor A20.D4 required for processive genome synthesis.
100 obscured by a complex multistep mechanism of processive GHs.
101                                              Processive glycoside hydrolases (GHs), like cellobiohydr
102                                              Processive glycoside hydrolases are the key components o
103 ylgalactosyl diacylglycerol synthesized by a processive glycosyltransferase.
104 se is synthesized by membrane-integrated and processive glycosyltransferases that polymerize UDP-acti
105 y electrophoresis shows that this PME is non-processive, halophilic, and acidophilic.
106           Kinesin-1, -2, -5, and -7 generate processive hand-over-hand 8-nm steps to transport intrac
107                     The structure suggests a processive hand-over-hand unfolding mechanism, where eac
108 molecule approaches, we show that hDNA2 is a processive helicase capable of unwinding kilobases of ds
109 stead as an adenosine triphosphate-dependent processive helicase when complexed with two accessory pr
110 itial binding, assembly, and function of the processive helicase-primase (primosome) component of the
111                                    PolC is a processive high-fidelity replicative polymerase, while t
112 osed of Cyclin T1 and CDK9, is essential for processive HIV-1 transcription.
113 We reveal that hKif15 is a plus-end-directed processive homotetramer that can step against loads of u
114 ays revealed that Pol beta scans DNA using a processive hopping mechanism and has a mean search footp
115  is involved in base excision repair, uses a processive hopping search mechanism to locate substrates
116  description of how this channel facilitates processive hydrolysis of unbound cAMP.
117 llably bidirectional myosin that is robustly processive in both forward and backward directions, and
118 core particles revealed that Pol beta is not processive in the context of a nucleosome, and its singl
119 the lagging-strand polymerase is simply less processive in the context of a replisome.
120 s suggest that phosphorylation can be pseudo-processive in the crowded cellular environment, since re
121 PC-mediated ubiquitylation involves a highly processive initial reaction on the substrate, followed b
122 n of (5m)C by CD of mouse TET2 is chemically processive (iterative).
123                      KIF3AB is an N-terminal processive kinesin-2 family member best known for its ro
124            Mammalian KIF3AB is an N-terminal processive kinesin-2 that is best known for its roles in
125                           KIF16B is a highly processive kinesin-3 family member that participates in
126 e affinity results in a high landing rate of processive kinesin-3 motors on the microtubule surface.
127 odimeric KIF17 and heterotrimeric KIF3AB are processive, kinesin-2 family motors that act jointly to
128 ficant reduction in the distances that these processive kinesins can travel.
129  tuned somewhat differently from homodimeric processive kinesins.
130 ity of KIF3AB in comparison with homodimeric processive kinesins.
131 ize, and a unified expression for predicting processive lifetime is revealed.
132 rocessive myosin ensembles and produce novel processive lifetime measurements.
133 s of prior experimental evidence that longer processive lifetimes are enabled by larger myosin ensemb
134 propose that secondary transport can adopt a processive-like mode of action, thus expanding the subst
135 ion by Mre11-Rad50-Xrs2 and Sae2, as well as processive long-range resection by Sgs1-Dna2 or Exo1 pat
136 plate and synthesize RNA product in a highly processive manner in vitro.
137 has also been reported to methylate DNA in a processive manner, a property that is incompatible with
138 d full deacetylation of (GlcNAc)3-6 in a non-processive manner.
139 quet, thus facilitating homolog pairing in a processive manner.
140 thesize that cleavage proceeds by means of a processive mechanism of substrate insertion, translocati
141 ed by RT0101 or RP027-028, consistent with a processive mechanism of trimethylation.
142 two CpG sites did not provide evidence for a processive mechanism over a wide range of enzyme concent
143                               This so-called processive mechanism relies on a complex pattern of enzy
144  first evidence that DHX36 uses a local, non-processive mechanism to unwind G4 substrates, reminiscen
145 dy state kinetic model that accounts for the processive mechanism.
146 the C-terminal domain that would allow for a processive mechanism.
147 Intracellular transport is largely driven by processive microtubule- and actin-based molecular motors
148 pulation undergo either diffusive, or highly processive, minus end-directed movements along microtubu
149 tor that can work alone, to Eg5, a minimally processive mitotic motor that works in large ensembles.
150 maining mutations selectively compromise the processive mode of dynein movement that is activated by
151 hanges the reaction from a distributive to a processive mode.
152                                     Teams of processive molecular motors are critical for intracellul
153  that unlike conventional myosin-II or other processive molecular motors, Ncd requires two ATP turnov
154 ects motor-microtubule complex stability and processive motility (the ability of an individual motor
155        Their slower chemical kinetics allows processive motility and a high stall force without the n
156  that a variety of adapter proteins activate processive motility by linking dynactin to dynein only w
157 ctional output of the K-loop with respect to processive motility of dimeric kinesin-3 motors is unkno
158                            Plus end-directed processive motility of KlpA on single microtubules depen
159                        Here, we examined the processive motility of mammalian dynein complexed with d
160 ppears to be well matched to the duration of processive motility of the KIF16B motor, indicating the
161              KlpA exhibits plus end-directed processive motility on single microtubules, but reverts
162                    This motor exhibited fast processive motility on single MTs interrupted by pauses.
163                                         This processive motility requires gating mechanisms to coordi
164 ing of LIS1 to DDB does not strongly disrupt processive motility.
165 lly required for an allosteric activation of processive motility.
166                 Central to understanding the processive motion of myosin on actin is the characteriza
167                Paradoxically, this resulting processive motion relies on quenching diffusive plasmid
168 ates that the origin of replication exhibits processive motion with a mean displacement that scales a
169 l of Cin8 is not necessary for bidirectional processive motion, but is controlling the switch between
170 the catalytic domain alone is sufficient for processive motion, providing insight into TrCel7A's mole
171 catastrophe inhibitor in vitro that uses its processive motor activity as part of a feedback loop to
172 tors, as well as with the requirement that a processive motor driving a large load via an elastic lin
173  the collective transport characteristics of processive motor enzymes in crowded conditions.
174 s in the natural intracellular medium, where processive motor enzymes might operate in crowded condit
175 shaped by evolution to cope with the lack of processive motor proteins in bacteria.
176 ess to explore the mechanochemical cycles of processive motor proteins such as kinesin-1, but it has
177 how that the mammalian kinesin-4 KIF21B is a processive motor that can accumulate at microtubule plus
178   Myosin 5c (Myo5c) is a low duty ratio, non-processive motor unable to move continuously along actin
179 he motor domain, KlpA is a plus end-directed processive motor; in contrast, when the tail detaches fr
180          The collective behaviors of certain processive motors, like myosinVa, may therefore be more
181 lity using assembling F-actin and two highly processive motors, myosin-5 and myosin-6.
182                         In contrast to other processive motors, stepping of the dynein motor domains
183                                        Thus, processive motors, which commonly follow individual prot
184 -type Myo52p with small cargoes, can undergo processive movement along actin-Cdc8p cables in vivo.
185 a transport machine capable of long-distance processive movement along microtubules.
186 how that the yeast kinesin-14 Kar3 generates processive movement as a heterodimer with the non-motor
187                             We observed that processive movement is rescued if ATP is added to the mu
188         The treadmilling dynamics direct the processive movement of the septal cell wall synthesis ma
189                The data suggest that, during processive movement, tethered-head binding occurs subseq
190  DNA scaffold is an important factor for the processive movement.
191  the coupling of two Myo5c molecules enables processive movement.
192 to a ternary complex (termed DDB) capable of processive movement.
193 tical trap loads, we observed staircase-like processive movements of myosin-10 interacting with the a
194       RNA localisation signals stimulate the processive movements, with regulation of dynein-dynactin
195                    The H3K4me3 mark promotes processive, multisite acetylation of histone H3 by Gcn5
196 neously binds a substrate-linked UB to drive processive multiubiquitination.
197 ational techniques are developed to simulate processive myosin ensembles and produce novel processive
198 trongly actin-bound states, similar to other processive myosin motors.
199 sin motor head promotes highly selective and processive myosin V.
200 mechanochemical systems are investigated for processive myosin-actin motility systems.
201                                      Natural processive myosins are dimeric and use internal tension
202 er, much of our mechanistic understanding of processive myosins comes from in vitro studies in which
203 -dependent ADP release that is essential for processive myosins, such as myosin V.
204            Importantly, our study shows that processive Nedd4-1, but not the distributive Nedd4-1:inh
205                Both human and yeast Exo1 are processive nucleases on their own.
206 corroborated by our observations that during processive nucleotide incorporation, sequential rounds o
207                                       During processive nucleotide incorporation, the first nucleotid
208  showed that human myosin Vc (MyoVc) was not processive on single-actin filaments [1-3].
209 ecords of motion reveal RNase R to be highly processive: one molecule can unwind over 500 bp of a str
210    We explored the possibility that MyoVc is processive only under conditions that resemble its biolo
211  to determine whether these knots arise by a processive or a dissociative mechanism.
212 val of phosphates can occur in a sequential (processive) or a stepwise (distributive) manner.
213 the initial step and also stimulates the two processive pathways, Sgs1-Dna2 and Exonuclease 1 (Exo1).
214            In contrast to Eg5, diffusive and processive periods were clearly distinguishable.
215         Because the latter monobody inhibits processive phosphorylation by Bcr-Abl and the SH2-kinase
216 harp contrast to the correlated rotations of processive PMEs, and the substrate-binding groove is neg
217 ferent behavior and properties compared with processive PMEs.
218 ication by varphi29 DNA polymerase, a highly processive polymerase enzyme that couples synthesis with
219 ding to the backside of certain E2s promotes processive polyUb formation, but the mechanism remains e
220                     More importantly, during processive primer extension, pyrophosphate (PPi) release
221  hypothesized that actin cables regulate the processive properties of MyoVc.
222           Active NicD contributes to the non-processive proteolysis and activation of BdlA via phosph
223 sted that individual motors are not robustly processive, raising questions about how dynein-associate
224                     This data supports for a processive, rather than distributed model of ERK phospho
225 otein splicing mediated by inteins is a self-processive reaction leading to the excision of the inter
226          Purified human telomerase catalyzes processive repeat synthesis, which could restore the ful
227 w model for DNA and RNA handling dynamics in processive repeat synthesis.
228                  This supports the idea that processive replication is required to maintain the histo
229          The chimeric polymerase carries out processive replication with PCNA in vitro; however, in y
230 , which mediate interactions with Pol31, and processive replication with the replication clamp prolif
231 erases depend on circular sliding clamps for processive replication.
232 ation of multiple Sec residues is inherently processive requiring only the SECIS elements but surpris
233 ion during homologous recombination-supports processive resection by Exo1.
234            Although this process is normally processive, resulting in the complete degradation of sub
235 ssociates into smaller particles, and begins processive retrograde IFT in <2 s.
236 ns but lack cytoplasmic dynein, the foremost processive retrograde transporter.
237                PcalRG is the most robust and processive reverse gyrase known to date; it is active ov
238                                              Processive, ring-shaped protein and nucleic acid protein
239 ndent RNA polymerase (RdRp), exhibits poorly processive RNA synthesis in vitro, at odds with the effi
240 Unlike their QDE-1(Ncr) counterpart favoring processive RNA synthesis, QDE-1(Tte) and QDE-1(Mth) prod
241                                    To ensure processive RNA synthesis, the viral polymerase L in comp
242 ter to transit into the elongation phase for processive RNA synthesis.
243 ear export dimerizes the motor and activates processive RNA transport.
244     Although polymerization is efficient and processive, RNase H is inefficient and periodic.
245 hen transmitted around the hexamer, reveal a processive rotary translocation mechanism and substrate-
246 ility datasets as a function of sample size, processive run length of the motor, and distribution of
247  KIF3AC heterodimer modulates entry into the processive run regardless of whether the run is initiate
248  this study, the kinetics for entry into the processive run were quantified.
249  KIF3AB heterodimer modulates entry into the processive run, and the results suggest that it is the h
250 uch that either KIF3A or KIF3C initiates the processive run.
251  that either KIF3A or KIF3C can initiate the processive run.
252 cycles of the two motor heads to sustain the processive run.
253 ation of motility during degradation reveals processive runs and distinct steps on the scale of 1 nm.
254 ation selectively destroys the initiation of processive runs at physiological ATP levels.
255 a series of gating mechanisms, which lead to processive runs averaging ~1 mum.
256 -1 function together to support fast, highly processive runs toward axon terminals.
257 gesting that the enzyme can initiate several processive runs without leaving the substrate.
258 e frequent and approximately fivefold longer processive runs, allowing them to catch up with leading
259      Myo1c also regulates the termination of processive runs.
260                           Application of our processive search assay into nucleosome core particles r
261                               We developed a processive search assay to determine if Pol beta has evo
262 logous DNA Pol X family members to perform a processive search for 1-nucleotide gaps in DNA using a p
263                  Of note, the differences in processive searching ability observed among the DNA Pol
264                                              Processive searching has been reported or proposed for m
265 nes within the lyase domain are required for processive searching, revealing a novel function for the
266                     We provide evidence that processive Sec incorporation is linked to selenium utili
267  exact order of these oxidation steps in the processive six-electron biosynthetic reaction is determi
268  nature of conformational changes leading to processive ssDNA translocation and multistranded DNA pro
269 NusG-like proteins to lock RNAP in a closed, processive state during elongation.
270                                  No signs of processive stepping at the single molecule level were ob
271 cule results presented show that the kinesin processive stepping distance decreases 40-60% with EC50
272 bability of rebinding to F-actin and enabled processive steps along actin filaments, which could be u
273 finity RING-E2 interactions result in highly processive substrate ubiquitination is largely unknown.
274       Telomerase helps maintain telomeres by processive synthesis of telomere repeat DNA at their 3'-
275 ep, which appears to be rate-limiting during processive synthesis.
276 nesin-1, with a shorter neck-linker, is more processive than kinesin-2.
277         Thus, although kinesin-1 may be more processive, the longer neck-linker length of kinesin-2 a
278 ses to remove base methylations and a highly processive thermostable group II intron reverse transcri
279 s or small molecules switches Nedd4-1 from a processive to a distributive mechanism of polyubiquitin
280 or of Nedd4-1, which switches Nedd4-1 from a processive to a distributive mechanism.
281 n human ribosomes during single-turnover and processive translation reactions.
282 hree tRNAs, which contributed to the rate of processive translation.
283 ngle molecule manifests during an individual processive translocation event.
284 anopores, a technique to unfold proteins for processive translocation has yet to be demonstrated.
285  is sufficient for gate activation, allowing processive translocation of export substrates for effici
286 illustrated by comparing kinesin-1, a highly processive transport motor that can work alone, to Eg5,
287 otor proteins that is critical for kinesin's processive transport of intracellular cargo along the mi
288 ulating dynein and kinesin motors to promote processive transport.
289 nonmuscle myosin IIB molecules form a highly processive unit when polymerized into filaments.
290          By generalizing a previous model of processive unwinding by helicases, we provide a unified
291 ed double-length SNARE complex, suggesting a processive unwinding mechanism.
292 on requires a RecQ dimer, and that continued processive unwinding of several kilobases involves multi
293 for RNA binding, subunit oligomerization and processive UTP incorporation, and predict druggable pock
294 rm tetramers and provide an amended model of processive VASP-mediated actin assembly in clustered arr
295 ubes and use that energy to fuel autonomous, processive walking through a series of conformational ch
296 bosomes glide forward on the mRNA track in a processive way.
297  limiting reaction regimes, distributive and processive, which differ in the number of enzyme-substra
298 sequence for coiled-coil formation is highly processive with run lengths of approximately 1.23 mum an
299  neck linker and helix alpha7 is also highly processive with run lengths of approximately 1.62 mum an
300 s translocation activity is rapid and highly processive, with individual complexes traveling an avera

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