ライフサイエンスコーパス: noncatalytic

1 nduced protein kinase SGK1; the mechanism is noncatalytic.

2 e of the substrate, phenylpyruvate (PPA), is noncatalytic.

3 role of VRK1 in neuronal migration is partly noncatalytic.

4 that A3G, A3F, and, to a lesser extent, the noncatalytic A3GC291S block human immunodeficiency virus

5 yze ring formation and thus may be more than noncatalytic accessory proteins.

6 opanoic acids or halides requires the use of noncatalytic acid promoters.

7 The possibilities for noncatalytic activation and the reversibility or irrever

8 ght on the regulation of their catalytic and noncatalytic activities in autophagy initiation.

9 subunits, and the ULK1 complex has essential noncatalytic activities.

10 formation through two genetically distinct, noncatalytic activities: activation of MamE-dependent pr

11 pecificity depends in part on binding of the noncatalytic ADAMTS13 spacer domain to the C-terminal al

12 Crk and CrkL are noncatalytic adaptor proteins necessary for the formatio

13 The organism is highly proteolytic, and noncatalytic adhesin domains of the major proteases, gin

14 binding and catalytic activity but promoted noncatalytic allosteric functions.

15 The noncatalytic alpha domain in the N-terminus appeared to

16 This tight fit places two noncatalytic amino acid residues, Phe-259 and Thr-314, w

17 ATPase domain of Cdc6 in the absence of the noncatalytic amino terminus is not sufficient for either

18 pression of either catalytic domain with the noncatalytic amino-terminal portion of HUGT1 conferred U

19 on required to induce PDR5 expression to the noncatalytic amino-terminal portion of Psd1.

20 The conservation of noncatalytic ancillary modules among these enzymes sugge

21 hanistically distinct active vaccines, i.e., noncatalytic and catalytic, for cocaine treatment.

22 e DinB tertiary structure suggests these are noncatalytic, and multiple-sequence alignments indicate

23 fold) in the hemostasis models tested than a noncatalytic antidote that is currently in clinical deve

24 phagosome deliver an array of catalytic and noncatalytic antimicrobial peptides, while activation of

25 coumarin-containing oligonucleotide and the noncatalytic APE1, the dye's absorption spectrum is shif

26 lution, 19 aaRSs expanded by acquiring novel noncatalytic appended domains, which are absent from bac

27 The noncatalytic B subunit of Shiga toxin 1 causes apoptosis

28 act with the redox polymer thus converts the noncatalytic base layer into a catalyst for the electror

29 Deletion of the homologue of the noncatalytic beta subunit in Schizosaccharomices pombe d

30 Hepatocystin functions as the noncatalytic beta subunit of Glucosidase II, an endoplas

31 catalytic alpha subunit and a homologous but noncatalytic beta subunit.

32 ermed "protein kinase C substrate 80K-H" or "noncatalytic beta-subunit of glucosidase II." This prote

33 tion of the APLTs, Dnf1p and Dnf2p, or their noncatalytic beta-subunit, Lem3p, blocked the import of

34 The noncatalytic betaGRPs may be evolutionarily derived from

35 ilico experiments reveal that stoichiometric noncatalytic binding and inhibition can generate a robus

36 In addition, we identify a unique, noncatalytic binding mode for the substrate bicarbonate

37 alytic sites, Pgamma is known to stimulate a noncatalytic binding of cGMP to the regulatory GAFa-GAFb

38 ependent formation of DMSOR(mod)D represents noncatalytic breakdown of the DMS species by a pathway a

39 n a highly conserved region that may serve a noncatalytic but essential function.

40 The enzyme-derived domains appear to be noncatalytic, but they determine the function of the two

41 Their interaction requires the kinase noncatalytic C-lobe domain (KIND) domain of Spire and th

42 t, is increased by interaction with the Nek9 noncatalytic C-terminal domain, suggesting a mechanism i

43 inducing a conformational change involving a noncatalytic C-terminal region spanning residues 414-551

44 Noncatalytic carbohydrate binding modules (CBMs) are com

45 Noncatalytic carbohydrate binding modules (CBMs) fulfill

46 ell wall degrading enzymes generally contain noncatalytic carbohydrate binding modules (CBMs) that fu

47 We previously reported that the noncatalytic carboxyl-terminal protein binding domain of

48 ly regulates the Sid1p kinase by binding the noncatalytic carboxyl-terminal region of the protein.

49 aTuSC depends on its kinase activity and its noncatalytic central domain.

50 The ability of Pgamma to stimulate noncatalytic cGMP binding to the GAF domains of PDE6 has

51 efect of H257N is not due to perturbation of noncatalytic cGMP binding to the PDE6alpha' GAF domains.

52 The noncatalytic cGMP-binding characteristics of the H257N m

53 s of PDE6 may lead to a stabilization of the noncatalytic cGMP-binding sites.

54 catalytic chain, Trm61, and a homologous but noncatalytic chain, Trm6, repurposed as a tRNA-binding s

55 es not distinguish between the catalytic and noncatalytic clades, and should be revised.

56 Moreover, and consistent with a noncatalytic clearance-based model for inhibition, appre

57 proteolytic ClpP proteins and four different noncatalytic ClpR proteins, with each present in one or

58 ana consists of five catalytic ClpP and four noncatalytic ClpR subunits.

59 (ORF15) C-terminal basic domain binds to the noncatalytic cofactor interaction domain unique to TTLL5

60 In Bacillus subtilis, P protein is the noncatalytic component of ribonuclease P (RNase P) that

61 mprising the C-terminal domains of E2p and a noncatalytic component, E3-binding protein (E3BP), which

62 rotein subunit (Est2p/TERT) and at least two noncatalytic components (Est1p and Est3p).

63 lectivity observed at low temperatures under noncatalytic conditions roughly predicts the regioselect

64 ntermediates in the catalytic reaction under noncatalytic conditions, suggest that N2 was reduced at

65 cyl-enzyme complexes has been acquired under noncatalytic conditions.

66 an intact polo-box, a conserved motif in the noncatalytic COOH-terminal domain of Cdc5, is required f

67 Surprisingly, we found that the two noncatalytic Cys around the active center exert an oppos

68 We hypothesize that noncatalytic cysteine pairs in Ero1p sense the level of

69 ted by attenuation of Ero1p activity through noncatalytic cysteine pairs.

70 be unperturbed from pK(a) values of typical noncatalytic cysteine residues.

71 cue flies that express either wild-type or a noncatalytic cysteine-serine mutant PGRP-SC1a, we find t

72 ased ligand design and covalent targeting of noncatalytic cysteines have been employed to develop pot

73 The noncatalytic DEP-GGL domain of RGS9 antagonized endogeno

74 Here, we show that ADAM11, a transmembrane noncatalytic disintegrin, is the first reported Kv1-inte

75 merization reaction, explain the role of the noncatalytic divalent cation in 6 RdRp, and pinpoint the

76 to form ternary complexes in the presence of noncatalytic divalent cations such as Ca(2+), Co(2+), Ni

77 ret these results to suggest that there is a noncatalytic docking site closely associated with PS1-ga

78 MTK1 has an extensive N-terminal noncatalytic domain composed of approximately 1,300 amin

79 l analysis suggests that the WNK1 C-terminal noncatalytic domain mediates vesicle localization.

80 The noncatalytic domain of ARF GAP1 was phosphorylated both

81 d protein with weak sequence similarity to a noncatalytic domain of class B penicillin-binding protei

82 adhesion kinase or with FRNK, the C-terminal noncatalytic domain of focal adhesion kinase, produced m

83 The amino-terminal noncatalytic domain of MKP-3 is both necessary and suffi

84 ERK binding to the N-terminal noncatalytic domain of MKP3 has been shown to increase (

85 We find that the noncatalytic domain of NHK-1 is crucial for its kinase a

86 romoting complex (APC)/cyclosome through the noncatalytic domain of Plo1 and the tetratricopeptide re

87 cytoplasmic domain, a transmembrane helix, a noncatalytic domain of unknown function, and a catalytic

88 ugu AID catalytic domain to the entire human noncatalytic domain restores activity in mammalian cells

89 motif was identified in the Nek2 C-terminal noncatalytic domain that allows both microtubule binding

90 ish the specific structural features of this noncatalytic domain that are essential to DNA conjugatio

91 ally associates with Cdt1 via its N-terminal noncatalytic domain, a region we had previously shown to

92 to membrane affinity: (1) the amino-terminal noncatalytic domain, and (2) a region with sequence simi

93 gesting that AID features mapping within the noncatalytic domain, but outside the NES, influence its

94 action motif (KIM) within its amino-terminal noncatalytic domain.

95 kinase activity or, surprisingly, any of the noncatalytic domain.

96 had lesions in one of eight residues in the noncatalytic domain.

97 of these large protein complexes consists of noncatalytic domains and subunits, and the ULK1 complex

98 r progressive and accretive proliferation of noncatalytic domains as the Tree of Life is ascended.

99 mechanisms involving both the catalytic and noncatalytic domains determine the distinct substrate sp

100 Noncatalytic domains may perform similar functions in ot

101 Additionally, noncatalytic domains of ADAM17 affected the size/shape o

102 We found that noncatalytic domains of ADAM17 did not directly bind the

103 This suggests that noncatalytic domains of ADAM17 play a role in substrate

104 Y(551) phosphorylation, and the role of the noncatalytic domains of Btk in the activation process.

105 Our results suggest a mechanism by which the noncatalytic domains of pollen-specific/enriched RopGEFs

106 f this study was to determine whether other, noncatalytic domains of RGS9-1.Gbeta5L enhance the intri

107 Therefore, noncatalytic domains of RGS9-1.Gbeta5L play a decisive r

108 ears to interact with both the catalytic and noncatalytic domains of the protease.

109 Splicing events retain noncatalytic domains while ablating the catalytic domain

110 ational modification of the protease, intact noncatalytic domains, and its cognate inhibitor.

111 With its noncatalytic domains, DNA-binding regions, and a catalyt

112 ation of the fXIa catalytic domain (CD) from noncatalytic domains.

113 alytic domains and more divergent C-terminal noncatalytic domains.

114 ckets or single residues, and into targeting noncatalytic domains.

115 attributed to multiple interactions between noncatalytic dynein subunits and an array of regulatory

116 een subunits, insights into the functions of noncatalytic editosome proteins, and a global understand

117 nitiate synaptic transmission and CaMKII has noncatalytic effects on presynaptic plasticity.

118 Because this indicated a potential noncatalytic ERK1/2 function, we generated stable lines

119 t DNA polymerase epsilon (Pol epsilon) has a noncatalytic essential role during the early stages of D

120 mutagenesis of ADAMTS-5 identified that the noncatalytic first thrombospondin and spacer domains med

121 BoNT/A(RYM) was noncatalytic for SNAP25 and nontoxic for mice.

122 tive mTP, indicating the conservation of the noncatalytic function across plant species.

123 lin D1 promotes cell cycle progression and a noncatalytic function has been described to sequester th

124 ulatory subunits of cohesin, implicating its noncatalytic function in inactivating cohesin's ability

125 These data show that FIG4 plays a critical noncatalytic function in maintaining lysosomal membrane

126 se observations suggest that SUS has a novel noncatalytic function in plant cells.

127 ing that this mammalian MAPK may also have a noncatalytic function in vivo.

128 The sensitizing mutation also impaired a noncatalytic function of Cdk2 in restricting assembly of

129 increased CDK2 activity associated with the noncatalytic function of CDK4, sequestration of p21(Cip1

130 ganisms, fully effective TLS also requires a noncatalytic function of the Y family polymerase REV1.

131 ere, we report that ERK1/2 also utilizes its noncatalytic function to mediate certain signal transduc

132 plasmic domain to uncouple the enzymatic and noncatalytic functions of CD45 in lymphocytes.

133 l surface, inhibiting both the catalytic and noncatalytic functions of LPL.

134 Both catalytic and noncatalytic functions of SHP2 are required for Fyn acti

135 e that these "pseudogenes" have alternative, noncatalytic functions that have not yet been uncovered.

136 that the EVH1 domain of Spred1 binds to the noncatalytic (GAPex) portion of the GAP-related domain (

137 Human CBS possesses a noncatalytic heme cofactor with cysteine and histidine a

138 The noncatalytic hemopexin domain of MMP9 binds to the low-d

139 on of both catalytically active ISA1 and the noncatalytic homolog ISA2.

140 dicots carry a pseudoenzyme PDX1.2 that is a noncatalytic homolog of the PDX1 subunit of the vitamin

141 Under noncatalytic (i.e., no H2 present) reaction conditions,

142 In our search for noncatalytic inhibitors of MT1-MMP, we compared the prot

143 bunit disulfide bonds were identified in the noncatalytic interaction domains; two in the MAM (meprin

144 ach of the related b and b' subunits, down a noncatalytic interface of the F1 domain and interacts in

145 l of mutual solvation of the partners of the noncatalytic "intimate" ion pair should release the nucl

146 unctional kinase, whereas phosphorylation of noncatalytic intracellular domains is required for recog

147 e second Glu was involved in binding a third noncatalytic ion in bacteriophage RB69 DNA polymerase.

148 mes (ISAs), including the catalytic ISA1 and noncatalytic ISA2, are major starch biosynthesis determi

149 For instance, the potato tuber enzyme has a noncatalytic L subunit that complements an S subunit wit

150 sphorylation of Ser(886) and Ser(999) in the noncatalytic linker connecting the synthetase cores.

151 Based on antibody binding experiments, the noncatalytic linker regions between the two enzymatic do

152 The noncatalytic lobe is anchored to the motor of the helica

153 t library by targeting imperfectly conserved noncatalytic loop residues and examined the effects on p

154 ug et al. propose a polyubiquitin-dependent, noncatalytic mechanism by which the deubiquitinase A20 i

155 Our results suggest a noncatalytic mechanism of IKK inhibition by A20 and a me

156 cell wall integrity signaling pathway uses a noncatalytic mechanism to activate the SBF (Swi4/Swi6) t

157 the yeast cell wall integrity pathway uses a noncatalytic mechanism to activate transcription of stre

158 1) and its pseudokinase paralog (Mlp1) use a noncatalytic mechanism to activate transcription of the

159 nts transport activity of MCT1 and MCT4 by a noncatalytic mechanism, while leaving transport activity

160 In summary, this PTEN noncatalytic missense mutation exposes a core tumor supp

161 Rp from bacteriophage varphi6 uses the bound noncatalytic Mn(2+) to facilitate the displacement of th

162 We find that this displacement releases the noncatalytic Mn(2+), which must be replaced for elongati

163 The additional noncatalytic module is therefore proposed to be required

164 Cel8 (SlCel9C1), with a distinct C-terminal noncatalytic module that represents a previously unchara

165 ing strategy that can identify catalytic and noncatalytic molecules that participate in different pat

166 mounts of sodium hydroxide needed to titrate noncatalytic montmorillonites as compared to the catalyt

167 It was noted that noncatalytic montmorillonites have a higher negative cha

168 In addition, a noncatalytic mutant (D210N) binds tightly to the same ol

169 In addition, structures of a noncatalytic mutant LC/A (Arg362Ala/Tyr365Phe) complexed

170 Noncatalytic mutations affecting the only cyclophilins w

171 We deleted the noncatalytic N and C termini in both GSK-3 isoforms and

172 Like other MKPs, MKP3 consists of a noncatalytic N-terminal domain and a catalytic C-termina

173 Deletion of the noncatalytic N-terminal domain led to loss of nucleolar

174 a dual-specificity phosphatase domain and a noncatalytic NH(2) terminus.

175 atalytic nucleotidyltransferase domain and a noncatalytic oligonucleotide/oligosaccharide binding (OB

176 associated with characterizing catalytic and noncatalytic outputs in cells, and describe successes an

177 ain insight into activating mutations in two noncatalytic p110alpha domains-the adaptor-binding and t

178 structural elements at the C terminus of the noncatalytic p51 subunit and the nucleic acid duplex in

179 nd the apicoplast of the genus Plasmodium, a noncatalytic paralog of ClpP, termed ClpR, has been iden

180 lization in a multisynthetase complex (MSC), noncatalytic peptide appendages, and ancillary functions

181 NORE1, a noncatalytic polypeptide, binds specifically to Ras-GTP

182 with either Cik1 or Vik1, both of which are noncatalytic polypeptides.

183 etion of PP1-87B or depletion of a conserved noncatalytic PP1 phosphatase subunit Sds22 leads to defe

184 hK1 and SphK2 depended on both catalytic and noncatalytic properties of Fyn.

185 ensional diffusion along protein surfaces, a noncatalytic protein bridge was inserted between GOx and

186 basis for a functional in vitro assay for a noncatalytic protein component of the telomerase complex

187 A variety of catalytic and noncatalytic protein domains are deployed by select micr

188 Nore1, a noncatalytic protein identified by its ability to bind s

189 Nore and RASSF1A are noncatalytic proteins that share 50% identity over their

190 tribution led us to report the first direct, noncatalytic quantitative observation of hydrogenolysis

191 bstrate, NAD+ and TbSIR2rp1 as follows: 1) a noncatalytic reaction between the deacetylation product

192 igomerization of benzylic compounds) and for noncatalytic reactions (Baeyer-Villiger oxidations, oxid

193 the mechanisms of signal initiation of this noncatalytic receptor, as well as to develop therapeutic

194 tive catalytic reduction (SCR) and selective noncatalytic reduction (SNCR) technology.

195 A noncatalytic reduction path on the Au surface and a cata

196 Plks are characterized by a C-terminal noncatalytic region containing two tandem Polo boxes, te

197 The mutations in mps1-8 are in the noncatalytic region of MPS1, and analysis of the mutant

198 to search for proteins with homology to the noncatalytic region of NIMA and identified mixed lineage

199 mic portion of ADAM17 through the C-terminal noncatalytic region of PLK2 containing the Polo box doma

200 mbinant SH3.1 domain of the adaptor molecule noncatalytic region of tyrosine kinase (Nck) can bind to

201 Although it is known that noncatalytic region of tyrosine kinase (Nck) regulates c

202 als that the KIM docking site, situated in a noncatalytic region opposite of the kinase catalytic poc

203 of these resemble NIMA within its extensive noncatalytic region, a region critical for NIMA function

204 kinetics led to the identification of three noncatalytic regions in MMP-1 (residues 285-295, 302-316

205 This binding supports the involvement of noncatalytic regions to the tight binding of the MK2:p38

206 s new structure supports the idea that these noncatalytic regions work together as a "conformational

207 ull-length kinase and the functional role of noncatalytic regions, we performed hydrogen-deuterium ex

208 alytic subunits (IKKalpha and IKKbeta) and a noncatalytic regulatory component named NEMO (NF-kappaB

209 Human mutations in KATNB1, which encodes the noncatalytic regulatory p80 subunit of katanin, cause se

210 reconstitution assay system, we now report a noncatalytic requirement for cyclin A-cdk2.

211 tion, a post-translational modification on a noncatalytic residue that increases its peroxidase activ

212 Interestingly, viruses with a mutation at a noncatalytic residue, D324A, could not be recovered desp

213 lutionary interactions between catalytic and noncatalytic residues have been difficult to define and

214 ytic metal-binding residues and two adjacent noncatalytic residues in LAGLIDADG homing endonucleases

215 s in favorable hydrogen bonds with conserved noncatalytic residues in the active site.

216 cale to create motifs of mixed catalytic and noncatalytic residues that identify enzyme activity and

217 ary for catalysis and structurally important noncatalytic residues that together maintain the archite

218 protein-DNA interactions is demonstrated by noncatalytic restriction mapping on a 4-kb DNA with thre

219 panosoma brucei which contains a degenerate, noncatalytic RNase III domain.

220 In yeast, Rev1 plays a noncatalytic role as an indispensable component of Polze

221 We identify a noncatalytic role for CD45 in regulating tonic, but not

222 omoted COPII assembly in vitro, suggesting a noncatalytic role for Nm23H2.

223 s support a model in which DBT plays a novel noncatalytic role in recruiting additional kinases that

224 Rev1's noncatalytic role in recruiting other DNA polymerases is

225 nt of the Polzeta-Rev1 complex, Rev1 plays a noncatalytic role in the association with DSBs.

226 uggest that cyclin A-cdk2 plays an ancillary noncatalytic role in the ubiquitination of p27 by the SC

227 ace-exposed region of one subunit while in a noncatalytic RT pocket of the other subunit.

228 The core of the cellulosome is a noncatalytic scaffoldin protein, which contains several

229 both the catalytic site and a portion of the noncatalytic, second phosphotyrosine binding site.

230 overexpression of the MST1 carboxy-terminal noncatalytic segment or by the NORE segment that binds M

231 and Nek7 (303AA), 76% identical, have little noncatalytic sequence but bind to the carboxyl-terminal

232 ivation of transcription by nitroalkenes via noncatalytic sequestration of these ligands, and their g

233 Here we show that the Anopheles gambiae noncatalytic serine protease CLIPA8, an essential factor

234 plex allosteric interactions involving their noncatalytic SH3 and SH2 domains.

235 is accessible by the optimal expression of a noncatalytic signaling component and that altering the e

236 or the i + 2 template position can bind to a noncatalytic site and increase the rate of RNA synthesis

237 demonstrates that L-serine binds to a second noncatalytic site and produces a conformational change i

238 oA levels, the binding of acyl-CoA with this noncatalytic site facilitates homotropic allosteric acti

239 The second, noncatalytic site for L-serine is likely to be the ASB d

240 nds to the active site and a unique proximal noncatalytic site formed by Lys-41, Arg-47, and Asp-48.

241 interact at either the catalytic site or the noncatalytic site interface.

242 e positions in which they exist at the three noncatalytic site interfaces in crystal structures.

243 tes the activity of another via binding to a noncatalytic site(s) rather than through binding to an a

244 y with the active site and a unique proximal noncatalytic site, we have recently acquired Compound 2,

245 ypsin-like activity by binding to a distinct noncatalytic site.

246 nucleotides or alters communication between noncatalytic sites and catalytic sites during ATP hydrol

247 duce a global effect that alters affinity of noncatalytic sites for nucleotides or alters communicati

248 Inhibitors that bind to noncatalytic sites of MMPs and disrupt protease signalin

249 e under conditions wherein binding of ATP to noncatalytic sites of the wild-type enzyme promotes rele

250 allosteric changes in cGMP binding to these noncatalytic sites on the enzyme.

251 escued by compensatory mutations at adjacent noncatalytic sites that restore an optimal coevolving ne

252 e high affinity cGMP binding to low affinity noncatalytic sites, and retard cGMP exchange with both n

253 Noncatalytic sites, such as those identified here, can u

254 e subunit were observed at its analogous but noncatalytic sites.

255 tic site during turnover when MgATP binds to noncatalytic sites.

256 re near the adenines of nucleotides bound to noncatalytic sites.

257 ic sites, and retard cGMP exchange with both noncatalytic sites.

258 o alphabeta is absent when cAMP occupies the noncatalytic sites.

259 In the heterodimeric enzymes, a noncatalytic small subunit (GPPS.SSU) determines the pro

260 CaPPS interacts with the noncatalytic spacer domain of ADAMTS-4 and the cysteine-

261 (1668) segment in the same domain and on the noncatalytic spacer domain of ADAMTS13, suggesting that

262 comprising a catalytic subunit (PriS) and a noncatalytic subunit (PriL).

263 in with one catalytic subunit (Kar3) and one noncatalytic subunit (Vik1).

264 of the proteasomes by interactions with the noncatalytic subunit alpha7 in a way that prevents the e

265 Each complex contains one catalytic and one noncatalytic subunit and exhibits endonuclease activity

266 uring NER requires the presence of a second, noncatalytic subunit called ERCC1.

267 its termed IKKalpha and IKKbeta as well as a noncatalytic subunit called IKKgamma/NEMO.

268 t-translationally by the availability of the noncatalytic subunit collagen Q, and others have shown t

269 alpha4 is an evolutionarily conserved noncatalytic subunit for PP2A-like phosphatases.

270 Polycomb group (PcG) repressor that is a key noncatalytic subunit in the ESC-Enhancer of zeste [E(Z)]

271 h synthase III (SSIII), and isa2, encoding a noncatalytic subunit of heteromeric isoamylase-type star

272 activated form of C3) on the function of the noncatalytic subunit of natural surface-bound forms of t

273 Here we show that alpha4, a noncatalytic subunit of protein phosphatase 2A (PP2A), i

274 In contrast, Psidin functions as the noncatalytic subunit of the N-acetyltransferase complex

275 Capns1 encodes the small noncatalytic subunit that is required for the proteolyti

276 NdmE is proposed to function as a noncatalytic subunit that serves a structural role in th

277 The noncatalytic subunit, Cdc50p, also was reconstituted in

278 re we report the identification of a primase noncatalytic subunit, denoted PriX, from the hyperthermo

279 serine kinases, IKKalpha and IKKbeta, and a noncatalytic subunit, IKKgamma.

280 alytic subunits, IKKalpha and IKKbeta, and a noncatalytic subunit, NF-kappaB essential modifier/IKKga

281 The IMP also has at least one noncatalytic subunit, Som1p, which is required to cleave

282 which we attribute to the differences in the noncatalytic subunit.

283 Diverged domains are present in the noncatalytic subunits and may be required for substrate

284 through concerted interactions with the two noncatalytic subunits in primer synthesis.

285 The noncatalytic subunits include p270/ARID1A, which is of p

286 B3GAP1 and RAB3GAP2 encode the catalytic and noncatalytic subunits of the hetrodimeric enzyme RAB3GAP

287 talytic SET domain subunit, E(Z), plus three noncatalytic subunits, SU(Z)12, ESC, and NURF-55.

288 a-proteobacteria-derived ancestors by adding noncatalytic subunits.

289 PRC2 modulation by conserved inputs from its noncatalytic subunits.

290 The complexes contain seven or more noncatalytic subunits; only one of which, hSNF5/Ini1/BAF

291 NIMA-like catalytic domain is followed by a noncatalytic tail containing seven repeats homologous to

292 c sequence but bind to the carboxyl-terminal noncatalytic tail of Nercc1/Nek9, a NIMA family protein

293 Noncatalytic targeting represents a novel approach to re

294 ogether, our data support the existence of a noncatalytic template-specific NTP binding site in the m

295 The results demonstrate that noncatalytic thrombospondin-1/cysteine-rich/spacer domai

296 ant stability vs metastability, catalytic vs noncatalytic transduction, pre- vs post-transcriptional

297 As, one enzyme homodimer plays a role of the noncatalytic unit that positions CCA ends of two tRNA(Se

298 between the globular domain of LpoB and the noncatalytic UvrB domain 2 homolog domain of PBP1B and m

299 id-solid growth and vertical facet-selective noncatalytic vapor-solid growth and their parallel integ

300 nsfer was fast enough to afford a reversible noncatalytic wave.