ライフサイエンスコーパス: ATP-dependent

1 and many bacterial and viral DNA ligases are ATP-dependent.

2 X5C and the import machinery was shown to be ATP-dependent.

3 The proteasome is an ATP-dependent, 2.5-megadalton molecular machine that is

4 Assays of cell lysates showed that ATP-dependent 5-oxoprolinase activity disappeared when p

5 Eukaryotes metabolize OP via an ATP-dependent 5-oxoprolinase; most prokaryotes lack homo

6 tant K487A had greatly reduced ATPase and no ATP-dependent ACOT activity.

7 as the enzyme responsible for catalyzing the ATP-dependent activation of MIA and MIA's attachment to

8 e cytoskeleton, intracellular membranes, and ATP-dependent active forces to intracellular mechanics a

9 We find that ATP-dependent activities enhance the nanoscale z fluctua

10 implies that some pseudokinases may possess ATP-dependent activities other than conventional phospho

11 ly chaperones, whose adenosine triphosphate (ATP)-dependent activity maintained the liquidity of shel

12 We show that the ATP-dependent activity of DHX36 arises from the RNA tail

13 We propose that the ATP-dependent activity of DHX36 may be useful for dynami

14 is proceeds through an ester generated by an ATP-dependent adenylating enzyme.

15 rocessing of the leader peptide and prior to ATP-dependent alternating access that translocates the c

16 The process is ATP dependent and can occur on pre- and post-translocati

17 regulates cardiovascular development through ATP-dependent and -independent activities, shedding ligh

18 Furthermore, DDX21 is both an ATP-dependent and ATP-independent helicase, and both ATP

19 he latest advances in understanding how both ATP-dependent and ATP-independent proteasome-regulated p

20 show that the DSB motion is subdiffusive and ATP-dependent and exhibits unique dynamical signatures,

21 within the Hel308 ATP hydrolysis cycle, one [ATP]-dependent and the other [ATP]-independent.

22 mple, reliable, and versatile method for the ATP-dependent assembly of evenly spaced nucleosome array

23 Chromatin undergoes a rapid ATP-dependent, ATM and H2AX-independent decondensation w

24 Here, we show that the ATP-dependent bacterial proteasome complex ClpXP degrade

25 quently used to study cross-presentation, is ATP-dependent but substantially TAP-independent.

26 n eIF3j affinity for the 43S PIC requires an ATP-dependent, but unwinding-independent, activity of eI

27 echanism in beige fat that involves enhanced ATP-dependent Ca(2+) cycling by sarco/endoplasmic reticu

28 We observed that phospholamban altered ATP-dependent calcium translocation by SERCA within the

29 trongly increased ATP substrate affinity and ATP-dependent catalytic velocity.

30 plicated in the regulation of a multitude of ATP-dependent cellular processes, exactly how these proc

31 Hsp90 is a dimeric ATP-dependent chaperone involved in the folding, maturat

32 k protein 70 (Hsp70) family member BiP is an ATP-dependent chaperone that plays a critical role in th

33 a hetero-oligomeric ClpPRT proteolytic core, ATP-dependent chaperones ClpC and ClpD, and an adaptor p

34 s from which native proteins are restored by ATP-dependent chaperones such as Hsp70 family members.

35 sHsps have been proposed to coordinate with ATP-dependent chaperones, including heat shock protein 7

36 o preferentially drive the expression of non-ATP-dependent chaperones.

37 stress resilience through high levels of the ATP-dependent chaperonin TRiC/CCT.

38 landscape shaped by adenosine triphosphate (ATP)-dependent chromatin remodeling and transcription.

39 Adenosine 5'-triphosphate (ATP)-dependent chromatin remodeling enzymes play essenti

40 e show that Uls1, an adenosine triphosphate (ATP)-dependent chromatin remodelling (Snf2) enzyme, can

41 The ATP-dependent chromatin assembly factor (ACF) spaces nuc

42 ayer in the fast kinetics of the NAD(+)- and ATP-dependent chromatin relaxation upon DNA damage in vi

43 ated with mutations in the gene encoding the ATP-dependent chromatin remodeler CHD7.

44 ayne syndrome cases contain mutations in the ATP-dependent chromatin remodeler CSB; however, how CSB

45 omatin remodeler family, and CSB is the only ATP-dependent chromatin remodeler essential for transcri

46 ome protein B (CSB) belongs to the SWI2/SNF2 ATP-dependent chromatin remodeler family, and CSB is the

47 helicase DNA-binding protein 4 (CHD4) is an ATP-dependent chromatin remodeler involved in epigenetic

48 licase DNA Binding Protein 1) is a conserved ATP-dependent chromatin remodeler that maintains the nuc

49 in helicase DNA binding protein 4 (CHD4), an ATP-dependent chromatin remodeler, acts as crucial coreg

50 We show that haploinsufficiency of the ATP-dependent chromatin remodeler, BAZ1B, which is delet

51 scription, and forms a complex with Brg1, an ATP-dependent chromatin remodeler, on the proximal promo

52 The SWI/SNF and RSC family of ATP-dependent chromatin remodelers disassembles nucleoso

53 Over the last 3 decades ATP-dependent chromatin remodelers have been thought to

54 ATP-dependent chromatin remodelers regulate chromatin dy

55 ecture of chromatin is governed, in part, by ATP-dependent chromatin remodelers.

56 by dynamic nucleosome unwrapping governed by ATP-dependent chromatin remodelers.

57 he expression of myogenic genes by promoting ATP-dependent chromatin remodeling and formation of tran

58 s one of the invariable core subunits of the ATP-dependent chromatin remodeling BAF (BRG1-associated

59 and RPL24, and with components of B-WICH, an ATP-dependent chromatin remodeling complex associated wi

60 ATP-dependent chromatin remodeling complexes are essenti

61 Accordingly, ATP-dependent chromatin remodeling complexes are importa

62 Among them, the ATP-dependent chromatin remodeling complexes control the

63 (Smarca5) are catalytic subunits of distinct ATP-dependent chromatin remodeling complexes implicated

64 Mammalian SWI/SNF complexes are ATP-dependent chromatin remodeling complexes that regula

65 ubstrate of Swi2/snif2-related 1 (SWR1), the ATP-dependent chromatin remodeling enzyme that deposits

66 n enzymatic subunit of the mammalian SWI/SNF ATP-dependent chromatin remodeling enzyme.

67 ibose to ATP, which supports the activity of ATP-dependent chromatin remodeling enzymes during hormon

68 odomain-helicase-DNA-binding (CHD) family of ATP-dependent chromatin remodeling enzymes, comprising C

69 ing is due to gene-specific requirements for ATP-dependent chromatin remodeling enzymes.

70 Here, we demonstrate that the ATP-dependent chromatin remodeling factor Snf2h (also kn

71 CHD7 encodes an ATP-dependent chromatin remodeling factor.

72 ATP-dependent chromatin remodeling factors of SWI/SNF2 f

73 chromodomain helicase DNA-binding family of ATP-dependent chromatin remodeling factors play essentia

74 Additionally, NAP1 histone chaperones, ATP-dependent chromatin remodeling factors, and some his

75 ATP-dependent chromatin remodeling proteins are being im

76 o transcription that can be relieved through ATP-dependent chromatin remodeling via complexes such as

77 ATP-dependent chromatin remodellers allow access to DNA

78 may act as a tunable interaction hotspot for ATP-dependent chromatin remodellers and, by extension, m

79 Recent observations suggest a role for ATP-dependent chromatin remodellers in modulating this p

80 ATP-dependent chromatin remodellers modulate nucleosome

81 ATP-dependent chromatin remodellers regulate access to g

82 pressor that couples histone deacetylase and ATP-dependent chromatin remodelling activities.

83 ATP-dependent chromatin remodelling enzymes (remodellers

84 ATP-dependent chromatin remodelling enzymes facilitate d

85 Here we show that the ATP-dependent chromatin remodelling INO80 complex promot

86 ATP-dependent chromatin-remodeling complexes utilize the

87 Significantly, our data identify that the ATP-dependent chromatin-remodeling enzyme Snf2 plays a f

88 ATP-dependent chromatin-remodeling enzymes control acces

89 Mutations in CHD7, encoding ATP-dependent chromodomain helicase DNA-binding protein

90 rs or trimers) and are loaded onto DNA by an ATP-dependent clamp loader complex that ruptures the int

91 ly conserved molecular chaperone involved in ATP-dependent client protein remodeling and activation.

92 Here, we show that the ATP-dependent complex of Pex1 and Pex6 from Saccharomyce

93 regulate MRX activity at DSBs by modulating ATP-dependent conformational changes of Rad50.

94 binding site near loop5, where it blocks the ATP-dependent conformational changes that we characteriz

95 one its clientele, Hsp90 proceeds through an ATP-dependent conformational cycle influenced by posttra

96 portant details underlying the links between ATP-dependent conformational dynamics and clients/cochap

97 Release of this direct interaction is ATP dependent, consistent with a transient eviction mech

98 previously, we observe a counteracting, and ATP-dependent, constriction of SecA around the pre-prote

99 isolated from myo2-E1-Sup1 are defective in ATP-dependent contraction in vitro.

100 a central metabolic enzyme and catalyses the ATP-dependent conversion of citrate and coenzyme A (CoA)

101 megadalton-sized complexes and catalyzes the ATP-dependent conversion of UMP to UDP in vitro with pro

102 mes may be used as a substrate for EutT, the ATP-dependent corrinoid adenosyltransferase and for the

103 proteins, BmbD and BmbE, responsible for the ATP-dependent cyclodehydration reactions that yield thia

104 Eukaryotic initiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase, is a critical compo

105 eukaryotic initiation factor 4A (eIF4A), an ATP-dependent DEAD-box RNA helicase; its messenger RNA s

106 cumented cytoplasmic roles as a modulator of ATP-dependent DEAD-box RNA helicases involved in messeng

107 previously known mevalonate pathways involve ATP dependent decarboxylation of either mevalonate 5-pho

108 athematical model of a highly generalisable, ATP-dependent, decision-making regulatory network, and s

109 ow YME1L recognizes substrates and catalyses ATP-dependent degradation has been hampered by the prese

110 and 6 in the D2 ring, work together to fuel ATP-dependent degradation is not understood.

111 proteasome is responsible for the selective, ATP-dependent degradation of polyubiquitinated cellular

112 nd the regulation of vital processes through ATP-dependent degradation of ubiquitinated substrates.

113 approved chemotherapeutic that stabilizes an ATP-dependent dimerization interface in topo II to block

114 g site on FlhG, their binding depends on the ATP-dependent dimerization state of FlhG.

115 ATP-dependent DNA end recognition and nucleolytic proces

116 yces cerevisiae Pif1 (ScPif1) is known as an ATP-dependent DNA helicase that plays critical roles in

117 ution of Mycobacterium tuberculosis LigD, an ATP-dependent DNA ligase dedicated to nonhomologous end

118 ase; Lhr-Core, a 3'-5' DNA helicase; LIG, an ATP-dependent DNA ligase; and Exo, a metallo-beta-lactam

119 The catalytic core of ATP-dependent DNA ligases consists of an N-terminal nucl

120 fd-dependent termination, the activity of an ATP-dependent DNA translocase that is thought to dissoci

121 strands, performed by a specialized class of ATP-dependent DNA translocases.

122 study also shows dramatic and unprecedented ATP-dependent DNA unwinding events by the M/R complex, w

123 replication without significantly affecting ATP-dependent duplex unwinding.

124 nin GroEL assists protein folding through an ATP-dependent encapsulation mechanism.

125 sis of pre-existing membrane (in addition to ATP-dependent endocytosis) to efficiently retrieve membr

126 ed in the replication stress response is the ATP-dependent endonuclease ZRANB3.

127 Chromatin remodelers are ATP-dependent enzymes that are critical for reorganizing

128 Here, we demonstrate the ATP-dependent, equilibrium binding of the cargo protein

129 which we find that BAF opposes PRC by rapid, ATP-dependent eviction, leading to the formation of acce

130 t mutant M41L/D67N/K70R/S215Y HIV-2 RT lacks ATP-dependent excision activity, and recombinant virus c

131 Thus, in addition to the long known ATP-dependent extraction of ERAD substrates during retro

132 s both necessary and sufficient to drive the ATP-dependent extraction of TA proteins from the membran

133 have isolated from extracts of HeLa cells an ATP-dependent factor that releases Cdc20 from MCC and id

134 he axon and slides them into alignment in an ATP-dependent fashion and then cross-links them in an AT

135 demonstrate that Srs2 disrupts D-loops in an ATP-dependent fashion and with a distinct polarity.

136 by CBP of H2A K5 and K8 in nucleosomes in an ATP-dependent fashion.

137 the catalytic component, MoFe-protein, in an ATP-dependent fashion.

138 g, while FlrA exclusively interacts with the ATP-dependent FlhG dimer and stimulates FlhG ATPase acti

139 tide binding activities, turning BiP from an ATP-dependent foldase into an ATP-independent holdase.

140 eine becomes oxidized, changing Kar2 from an ATP-dependent foldase to an ATP-independent holdase.

141 A detailed structural understanding of its ATP-dependent folding mechanism and substrate recognitio

142 he first step of the replicase reaction: the ATP-dependent formation of an initiation complex between

143 d-alanine-d-alanine ligase (Ddl), catalyzes ATP-dependent formation of the d-alanyl-d-alanine dipept

144 ociated herpesvirus (KSHV), by targeting the ATP-dependent formation of viral ribonucleoprotein parti

145 enzymology" approach, we (i) assigned novel ATP-dependent four-carbon acid sugar kinase functions to

146 sis has been generally recognized as a major ATP-dependent function, which efficiently retrieves more

147 ould be overcome in a specific manner by the ATP-dependent G4-resolving helicase Pif1.

148 the potency of ATP at stimulating current or ATP-dependent gating when ATP was the only nucleotide pr

149 TP-independent helicase, and both ATPase and ATP-dependent helicase activities are inhibited by Rev i

150 6, also known as RHAU or G4R1, is a DEAH-box ATP-dependent helicase highly specific for DNA and RNA G

151 a pigmentosum group D (XPD/ERCC2) encodes an ATP-dependent helicase that plays essential roles in bot

152 Here, we describe a new role for the ATP-dependent helicase UPF1 and its interaction with the

153 promising dependencies, the Werner syndrome ATP-dependent helicase, as a synthetic lethal target in

154 s granules and human diseases and identifies ATP-dependent helicases and protein remodelers as conser

155 We discovered ATP-dependent histone H2A acetylation activity in Drosop

156 gregation and facilitates their refolding by ATP-dependent Hsp70-Hsp100 disaggregases.

157 Here, we show that an ATP-dependent human chaperone system disassembles Tau fi

158 s the pyridine salvage route resulting in an ATP-dependent increase of intracellular NAD(+).

159 hannel entrance and promoting its subsequent ATP-dependent insertion.

160 ous action potentials even in the absence of ATP-dependent intercellular Ca(2+) signaling in the nons

161 fire spontaneous APs even in the absence of ATP-dependent intercellular Ca(2+) signalling in the non

162 reveal a protein kinase fold that catalyzes ATP-dependent isopeptide bond formation between the amin

163 KdpFABC is an ATP-dependent K(+) pump that ensures bacterial survival

164 precursor to NAD(+) Cell lysates possess an ATP-dependent kinase activity that efficiently converts

165 the members of the DUF1537 family are novel ATP-dependent kinases that participate in catabolic path

166 UDP-stimulated phagocytic activity, and the ATP-dependent laser lesion-induced process outgrowth.

167 ermini required for sealing by an N-terminal ATP-dependent ligase domain (LIG).

168 and outer leaflets of the plasma membrane by ATP-dependent lipid transporters.

169 nally remodel specific target proteins in an ATP-dependent manner is not well understood.

170 ty is imported into phagosomes in a TAP- and ATP-dependent manner, as expected.

171 hich facilitate protein disaggregation in an ATP-dependent manner, determines the lag time for bacter

172 the fly ortholog of H2A.Z) genome-wide in an ATP-dependent manner, like the yeast SWR1 complex.

173 ks DNA plectonemes and can compact DNA in an ATP-dependent manner.

174 nin system facilitates protein folding in an ATP-dependent manner.

175 form clusters that condense DNA in a weakly ATP-dependent manner.

176 sylates (thus removing -SNO) from Prx2 in an ATP-dependent manner.

177 presses replication of certain viruses in an ATP-dependent manner.

178 eir folding within an isolated chamber in an ATP-dependent manner.

179 cids, HelD dissociates from the enzyme in an ATP-dependent manner.

180 ex structures and unwinds DNA duplexes in an ATP-dependent manner.

181 s macroH2A1.2 and macroH2A2 deposition in an ATP-dependent manner.

182 reveal that respiratory restriction inhibits ATP-dependent matrix processes that are critical for mit

183 CFTR intraburst gating is distinct from the ATP-dependent mechanism that controls channel opening an

184 understanding of the proteasome's multistep ATP-dependent mechanism, its biochemical and structural

185 c (proopiomelanocortin; POMC) neurons via an ATP-dependent mechanism.

186 To explore how oxidative stress and ATP-dependent metabolism affect mitochondria, experiment

187 NDL1 encodes a mitochondria-localized ATP-dependent metalloprotease belonging to the FILAMENTA

188 en Staphylococcus aureus, the membrane-bound ATP-dependent metalloprotease FtsH plays a critical role

189 FTSH4 is one of the inner membrane-embedded ATP-dependent metalloproteases in mitochondria of Arabid

190 mination or elongation rescue, which rely on ATP-dependent Mfd translocation on DNA.

191 phosphate decarboxylases (MDDs) catalyze the ATP-dependent-Mg(2+)-decarboxylation of mevalonate-5-dip

192 Hsp90 is a homodimeric ATP-dependent molecular chaperone that remodels its subs

193 (Hsp70) are two families of highly conserved ATP-dependent molecular chaperones that fold and remodel

194 ss in which DNA sequences are aligned via an ATP-dependent molecular motor-driven mechanism.

195 nstrate that both condensin I and II exhibit ATP-dependent motor activity and promote extensive and r

196 attachment sites were observed: the typical ATP-dependent motor domain attachment and a novel ATP-in

197 Rad54 and Rdh54 are closely related ATP-dependent motor proteins that participate in homolog

198 e double-stranded DNA (dsDNA) viruses use an ATP-dependent motor to drive DNA into preformed capsids.

199 reorganization is for an ssDNA translocase (ATP-dependent motor) to push the SSB along ssDNA.

200 litate protein folding by undergoing energy (ATP)-dependent movements that are coordinated in time an

201 decrease in Vmax and increase in KM for the ATP-dependent NADHX dehydratase activity.

202 Hsp70 molecular chaperones are abundant ATP-dependent nanomachines that actively reshape non-nat

203 a bacterial DNA topoisomerase that catalyzes ATP-dependent negative DNA supercoiling and DNA decatena

204 ecA-like domains (D1D2), DDXs function in an ATP-dependent, non-processive manner.

205 ParA binds to the bacterial nucleoid via an ATP-dependent nonspecific DNA (nsDNA)-binding activity,

206 This unwinding activity is achieved by the ATP-dependent nonstructural protein 3 (NS3) helicase.

207 end joining was promoted by both ATM and the ATP-dependent nucleosome remodeler INO80.

208 SIN mutation that bypasses the need for the ATP-dependent nucleosome remodeler SWI/SNF) leads to mit

209 otal role in transcriptional regulation, and ATP-dependent nucleosome remodeling activity is required

210 We have investigated the role of the SWI/SNF ATP-dependent nucleosome-remodeling complex in the repai

211 loop and conserved in McdA homologs, enables ATP-dependent nucleotide sandwich dimer formation.

212 In addition to the ATP-dependent opening of SecY, reported previously, we o

213 ludes microglia-specific processes including ATP-dependent P2X4 and P2X7 activation, activation of nu

214 By contrast, (ATP-dependent) PfkA of Escherichia coli, which does rely

215 ATP-dependent phospholipid flippase activity crucial for

216 s a membrane-bound enzyme that catalyzes the ATP-dependent phosphorylation of diacylglycerol to form

217 thiamine pyrophosphate (TPP) synthesis, the ATP-dependent phosphorylation of thiamine monophosphate

218 The Kif18A motor domain drives ATP-dependent plus-end microtubule gliding, and undergoe

219 s the Rnl5 family of adenosine triphosphate (ATP)-dependent polynucleotide ligases that seal 3'-OH RN

220 esence of glibenclamide, an inhibitor of the ATP-dependent potassium (KATP)-channels, thus suggesting

221 ives heme insertion into apoprotein-Mb in an ATP-dependent process.

222 eolus-nucleoplasm interface is maintained by ATP-dependent processes and susceptible to changes in ch

223 that cells control RNA condensation through ATP-dependent processes, static RNA buffering, and dynam

224 a stable complex with Pol II and acts as an ATP-dependent processivity factor that helps Pol II acro

225 ptor protein ClpS, an essential regulator of ATP-dependent protease ClpAP, directly interacted with P

226 ClpXP is an ATP-dependent protease in which the ClpX AAA+ motor bind

227 e them resistant to enzymatic degradation by ATP-dependent proteases and recent studies have shown th

228 ATP-dependent proteases translocate proteins through a n

229 anced ATPase activity, peptide cleavage, and ATP-dependent protein degradation.

230 es, ClpX or ClpC1, thus inhibiting essential ATP-dependent protein degradation.

231 li comprises GroEL and GroES and facilitates ATP-dependent protein folding in vivo and in vitro Prote

232 ous molecular chaperone that participates in ATP-dependent protein remodeling in both eukaryotes and

233 ospholipids allosterically activate SecA for ATP-dependent protein translocation.

234 and archaeal branches.Chaperonins (CPNs) are ATP-dependent protein-folding machines.

235 wn to participate in adenosine triphosphate (ATP)-dependent proteolysis in bacteria.

236 proteins show substrate-specific defects in ATP-dependent proteolysis.

237 rbonylated proteins in ftsh4 was the limited ATP-dependent proteolytic capacity of ftsh4 mitochondria

238 (+)-ATPase (V-ATPase; V(1)V(o)-ATPase) is an ATP-dependent proton pump that acidifies subcellular com

239 The vacuolar H(+)-ATPase (V-ATPase) is an ATP-dependent proton pump that is essential for cellular

240 ansporter P-glycoprotein (P-gp, ABCB1) is an ATP-dependent pump that mediates the efflux of structura

241 d cyclic nucleotide-gated channels, and from ATP-dependent pumping of Ca(2+) entering voltage-gated c

242 active KCC2-mediated chloride extrusion, and ATP-dependent pumps.

243 Similar ATP-dependent pushing events, but in the opposite (3' to

244 e (LplJ) that catalyzes a classical two-step ATP-dependent reaction.

245 case disassembles the leading ribosome in an ATP-dependent reaction.

246 glutamine to asparagine and glutamate in an ATP-dependent reaction.

247 f Hsp70 and ClpB/Hsp104 chaperones, which in ATP-dependent reactions disentangle individual proteins

248 sponse indicative of a specific hierarchy of ATP-dependent reactions.

249 DEAD-box helicase proteins perform ATP-dependent rearrangements of structured RNAs througho

250 Nitrogenase catalyzes the ATP-dependent reduction of dinitrogen (N2) to two ammoni

251 -independent unfolding of G4-RNA followed by ATP-dependent refolding, generating a highly asymmetric

252 -modified macromolecules efficiently inhibit ATP-dependent release of interleukin-1beta from human an

253 involvement of Alc1, a poly(ADP-ribose)- and ATP-dependent remodeler, in the chromatin-relaxation pro

254 This is in part overcome by enzymes, termed ATP-dependent remodelers, that are recruited to nucleoso

255 the interplay between the transcriptome and ATP-dependent remodeling in SG formation.

256 ay contribute to chromatin regulation beyond ATP-dependent remodeling.

257 uffering ensures nucleosome stability during ATP-dependent remodelling, and provides a means for comm

258 I action that is distinct from that of other ATP-dependent restriction-modification enzymes.

259 de duplex annealing, adenosine triphosphate (ATP)-dependent RNA binding, and RNA-protein complex remo

260 iochemical assays demonstrated that it is an ATP-dependent RNA and DNA helicase.

261 We demonstrate that, through ATP-dependent RNA binding, the DEAD-box protein eIF4A re

262 and potentially other DEAD-box proteins, as ATP-dependent RNA chaperones that limit the condensation

263 zymes polynucleotide phosphorylase (PNPase), ATP-dependent RNA helicase (RhlE), ribonuclease E (RNase

264 The enzyme possesses an intrinsic, ATP-dependent RNA helicase activity that is essential in

265 associated with AU-rich element (RHAU) is an ATP-dependent RNA helicase that demonstrates high affini

266 e or AGO2-loaded miRNAs does not require the ATP-dependent RNA helicase UPF1 in vitro, we report here

267 Consequently, a substrate of SMG1, ATP-dependent RNA helicase upframeshift 1, is hyperphosh

268 eIF4G (a scaffolding subunit) and eIF4A (an ATP-dependent RNA helicase) leads to assembly of active

269 al structures of the founding members of the ATP-dependent RNA ligase family (T4 RNA ligase 1; Rnl1)

270 An ATP-dependent RNA ligase from Methanobacterium thermoaut

271 These findings suggest that ATP-dependent RNA ligase may act on a specific set of 3'

272 ngal Trl1 as the founder of an Rnl6 clade of ATP-dependent RNA ligase.

273 d Glu285, which are conserved among archaeal ATP-dependent RNA ligases and are situated on the surfac

274 h segment; termination by the enzyme Rho, an ATP-dependent RNA translocase that releases RNA by forci

275 The DEAD-box family of proteins are ATP-dependent, RNA-binding proteins implicated in many a

276 p97 is a ubiquitin-targeted ATP-dependent segregase that extracts ubiquitylated clie

277 In addition to its ATP-dependent severing activity, spastin is an ATP-indep

278 complexes that in general comprise a central ATP-dependent Snf2 family helicase that is decorated wit

279 oter, and O-GlcNAc removal from pol II is an ATP-dependent step during initiation.

280 needs to be revised to include an additional ATP-dependent step.

281 We identify this rotary step as the ATP-dependent substep, and find that the associated free

282 e removed by the deubiquitinase Rpn11 during ATP-dependent substrate degradation.

283 amily members (ERdjs), which stimulate BiP's ATP-dependent substrate interactions, with several ERdjs

284 n, beyond which strand passage competes with ATP-dependent supercoil relaxation.

285 let beta-cell function are controlled by the ATP-dependent Swi/Snf chromatin remodeling coregulatory

286 ects of TRF are mediated by circadian clock, ATP-dependent TCP/TRiC/CCT chaperonin and mitochondrial

287 lism and pyruvate dehydrogenase activity for ATP-dependent thermogenesis through the SERCA2b pathway;

288 al temporal autocorrelation functions reveal ATP-dependent transient short-range (<2 mum) heterogenei

289 single-molecule imaging to determine how the ATP-dependent translocase RecBCD travels along DNA occup

290 ly of serine proteases that collaborate with ATP-dependent translocases to degrade protein substrates

291 single turnover kinetics to investigate the ATP-dependent translocation of soluble polypeptides by H

292 integrate with conserved motifs required for ATP-dependent translocation to unfold and degrade target

293 codes the alpha-subunit of a neuron-specific ATP-dependent transmembrane sodium-potassium pump.

294 s with the motor protein SecA to mediate the ATP-dependent transport of pre-proteins across the membr

295 The dependence of ATP-dependent transport on proton coupling, and the stim

296 P-glycoprotein (P-gp) is a polyspecific ATP-dependent transporter linked to multidrug resistance

297 Deletion of the ATP-dependent transporter, CbpD partially alleviated xyl

298 and ClpP2 subunits, and hexameric ring-like ATP-dependent unfoldases composed of ClpX or ClpC1.

299 Here, we show that IvoA catalyzes ATP-dependent unidirectional stereoinversion of l-trypto

300 Brr2 catalyzes an ATP-dependent unwinding of the U4/U6 RNA duplex, which i