ライフサイエンスコーパス: oligomerization

1 ation, nitration, inactivation, and covalent oligomerization.

2 use model, we artificially enhanced alphaSyn oligomerization.

3 in regulating RR specificity, allostery, and oligomerization.

4 ing CRY2-CRY2 interaction prefer robust homo-oligomerization.

5 nhibits kinase activity by reducing receptor oligomerization.

6 Cry1Ac interaction with cadherin triggers oligomerization.

7 hology is through a major role of decreasing oligomerization.

8 t opening of the complex is prerequisite for oligomerization.

9 structures, and three are involved in DISC1 oligomerization.

10 namics that serves as a regulator for MFN1/2 oligomerization.

11 reover, G4 substrates induce cooperative AID oligomerization.

12 t relies on unfolded protein binding-induced oligomerization.

13 stereochemistry at the C3 carbon can induce oligomerization.

14 t the post-translational level by FRP and/or oligomerization.

15 Delta) mutation, which promotes amyloid-beta oligomerization.

16 y of tandem GFP11-tag in scaffolding protein oligomerization.

17 R1 at the plasma membrane and facilitate its oligomerization.

18 h Fam65b in stereocilia and regulates Fam65b oligomerization.

19 l GXXXG in putative TM2 is important for S1R oligomerization.

20 interactions are essential in preformed Tie2 oligomerization.

21 stable, well-folded and undergoes reversible oligomerization.

22 cofactor binding, allosteric activation and oligomerization.

23 cross-linked peptides, which indicated Atg18 oligomerization.

24 ped in a compact conformation preventing its oligomerization.

25 ng contacts with the minor groove of DNA and oligomerization.

26 d induce allosteric changes that lead to its oligomerization.

27 s much larger configurations consistent with oligomerization.

28 -36) monomer (2) interfere with Abeta(17-36) oligomerization (3) disrupt a pre-formed Abeta(17-36) pr

29 In addition, IRE1alpha oligomerization, activation, and inactivation during ER

30 9, and this association triggered their homo-oligomerization/activation.

31 and S16) towards huntingtin exon 1 (HTTex1) oligomerization, aggregation and toxicity in human cells

32 mini and the hook region of beta1a prevented oligomerization, allowing for its structural determinati

33 -core motifs of this defensin that eliminate oligomerization also knockout its ability to induce memb

34 as screened to identify antagonists of Abeta oligomerization, amyloid formation, and cytotoxicity.

35 Misfolding, oligomerization and accumulation of the human alpha-synu

36 However, the coupling of ER stress to IRE1 oligomerization and activation has remained obscure.

37 phrinA1, a ligand for EphA2, induced further oligomerization and activation of EphA2FL-GFP.

38 Several studies point to alpha-syn oligomerization and aggregation as a mediator of neuroto

39 in protein stability and then the subsequent oligomerization and aggregation.

40 We studied the oligomerization and albumin-binding of the unconjugated

41 tamate formation increases the rate of Abeta oligomerization and alters the interactions of Abeta wit

42 h effector four-helical bundle of MLKL, (ii) oligomerization and association of MLKL with cellular me

43 ngth Spa47 point mutants, we find that Spa47 oligomerization and ATP hydrolysis are needed for comple

44 mational mutp53s bypass Akt to induce TopBP1 oligomerization and attenuate ATR checkpoint response du

45 ured linker region connecting the N-terminal oligomerization and C-terminal DNA binding domains.

46 nding site are required for PA-mediated NsD7 oligomerization and coil formation, as well as permeabil

47 inal tripartite motifs (TRIM), which mediate oligomerization and create avidity effects.

48 ously undergo light-dependent CRY2-CRY2 homo-oligomerization and CRY2-CIB1 hetero-dimerization, both

49 ccepted role in aiding S-layer biogenesis or oligomerization and demonstrates a connection to cellula

50 of Roco proteins and suggests a link between oligomerization and disease-associated mutations in LRRK

51 show that 5 effectively inhibits both Abeta oligomerization and fibrillation.

52 ily conserved protein is necessary for Cox15 oligomerization and function.

53 t to fuse adjacent mitochondria via combined oligomerization and GTP hydrolysis.

54 LRP3 and AIM2 inflammasome by preventing ASC oligomerization and may be a potential therapeutic candi

55 rization, with positive charges facilitating oligomerization and negative charges inhibiting it.

56 edominantly comes from the disruption of DR5 oligomerization and not ligand sequestration.

57 l domain of A3G (A3G-CD1) is responsible for oligomerization and nucleic acid binding, both of which

58 he first time, that ABCC2 facilitates Cry1Ac oligomerization and oligomer membrane insertion in P. xy

59 ssome, determinants for RNA binding, subunit oligomerization and processive UTP incorporation, and pr

60 ymerase subunit PB2 and phospho-regulates NP oligomerization and RNP assembly during infection.

61 21-mediated p62 ubiquitylation abrogates p62 oligomerization and sequestration of proteins including

62 -dependent p53 modulation requires both auto-oligomerization and tandem-BRCT domain-mediated bivalent

63 ze that sHsp chaperone efficiency depends on oligomerization and that client interactions can occur b

64 However, the structural basis of homo-oligomerization and the fractional distribution of oligo

65 T-23, which promotes actin-dependent dynamin oligomerization and thus, increases actin polymerization

66 of the lipid membrane composition on protein oligomerization and to observe structural changes in pro

67 orrect membrane insertion, tertiary folding, oligomerization, and biochemical modification of the new

68 ciated speck-like protein with a CARD domain oligomerization, and caspase-1 processing, key events du

69 tivation of HK activity via homo- and hetero oligomerization, and cross-phosphorylation between HKs.

70 mechanisms, including scaffolding, wedging, oligomerization, and crowding.

71 ynamin function and couple membrane binding, oligomerization, and GTPase activity during dynamin-cata

72 on constrain AtHIR1 dynamics, promote AtHIR1 oligomerization, and increase the efficiency of the inte

73 essibility of Abeta1-42 at various stages of oligomerization, and provides new insights on site-speci

74 ding to their catalytic active site, protein oligomerization, and substrate specificity.

75 omers, the cysteine residues involved in the oligomerization appear to be different.

76 Binding to RhoC and oligomerization are critical for Fam65b function.

77 intracellular amyloid-beta accumulation and oligomerization are early AD pathologic processes, which

78 In addition, neurabin domains required for oligomerization are essential for formation of the A1R/n

79 y intermediates in olefin polymerization and oligomerization, are presented.

80 s the current state of our knowledge of MDM2 oligomerization as well as current efforts to target the

81 A (e.g., matrix and nucleocapsid) impact Gag oligomerization as well as immature particle size and mo

82 disrupt bifurcated substrate recognition or oligomerization both compromise CSR in splenic B cells.

83 Notably, ligand binding also induces EGFR oligomerization, but the structures and functions of the

84 y, consistent with netrin-1-induced receptor oligomerization, but with no change in aggregation state

85 nd to strongly impact on protein folding and oligomerization by altering the hydrogen bond network.

86 we analyzed Cry1Ac and Cry1AcMod binding and oligomerization by western blots using brush border memb

87 in Nature Cell Biology, show how PAR protein oligomerization can dynamically couple protein diffusion

88 ling protocols, we further targeted ethylene oligomerization catalysis by Ni-AIM guided by theoretica

89 Spc110/Spc72 and Mzt1 constitute "oligomerization chaperones," cooperatively promoting and

90 domain deletion (EphA2DeltaS-GFP) increases oligomerization compared to the full length receptor (Ep

91 QUC reduced ASC speck formation and ASC oligomerization compared with controls.

92 ly phosphorylates ASC and brings ASC into an oligomerization-competent state by allowing Tyr146 phosp

93 in lipid bilayers and forms a viroporin upon oligomerization, confirmed by EIS conductance measuremen

94 SAF-A oligomerization decompacts large-scale chromatin structu

95 nd oligomerization kinetics of wild-type and oligomerization-deficient A3G, and find that A3G first t

96 ersisted, but trans-allostery was lost in an oligomerization-deficient GLUT1 variant in which we subs

97 either alanine or glutamine severely reduces oligomerization, demonstrating the role of protonated E7

98 ion of ExoU and that this PI(4,5)P2-mediated oligomerization does not require ubiquitin.

99 Activation of nucleotide-binding oligomerization domain (NOD) 1 and NOD2 by muropeptides

100 masome, by members of the nucleotide-binding oligomerization domain (Nod), leucine-rich repeat-contai

101 ponse pathways, including nucleotide-binding oligomerization domain (NOD)-, Toll-, and RIG1-like rece

102 Nucleotide-binding oligomerization domain (Nod)-containing proteins Nod1 an

103 ing 1 (NLRP1), NLRP3, and nucleotide-binding oligomerization domain (NOD)-like receptor C4 (NLRC4) we

104 Nucleotide-binding oligomerization domain (NOD)-like receptor family, pyrin

105 mmation by activating the nucleotide-binding oligomerization domain (NOD)-like receptor protein 3 (NL

106 stem was not dependent on nucleotide binding oligomerization domain (NOD)-like receptors (NLRs), reti

107 Nucleotide-binding and oligomerization domain (NOD)-like receptors NOD1 and NOD

108 A chimeric RABV P protein in which the oligomerization domain (OD) and the CTD were replaced by

109 the helicase domain of Rep68 as a bona fide oligomerization domain (OD).

110 PV) forms homotetramers composed of a stable oligomerization domain (Pcore) flanked by large intrinsi

111 cognition receptor, NOD2 (nucleotide-binding oligomerization domain 2), belongs to the innate immune

112 ymbiotic bacteria via the nucleotide-binding oligomerization domain containing 2 (Nod2) sensor in cel

113 trate that both TNF-R and nucleotide-binding oligomerization domain stimulation promote ATG16L1 stabi

114 VP35 contains a central oligomerization domain with a predicted coiled-coil moti

115 table helices are formed C terminally to the oligomerization domain, extremely transient helices are

116 The inflammasome proteins nucleotide-binding oligomerization domain, leucine rich repeat and pyrin do

117 ceptor (IL-1R) family and nucleotide-binding oligomerization domain, leucine-rich repeat and pyrin do

118 se susceptibility protein nucleotide-binding oligomerization domain-containing 2 (NOD2); however, the

119 enhanced by activation of nucleotide-binding oligomerization domain-containing protein (NOD) 2.

120 Nucleotide-binding oligomerization domain-containing protein 1 (NOD1) is a

121 he innate immune receptor nucleotide-binding oligomerization domain-containing protein 2 (NOD2) is es

122 e signaling-3, rs4969170; nucleotide-binding oligomerization domain-containing protein 2, rs3135500;

123 n (CARD)-containing member of the nucleotide oligomerization domain-like receptor (NLR) family, was f

124 ne 1-like receptor (RLR), nucleotide-binding oligomerization domain-like receptor (NLR), and Toll-lik

125 Excessive nucleotide-binding oligomerization domain-like receptor family, pyrin domai

126 protein kinase, Jak-STAT, and the nucleotide oligomerization domain-like receptor pathways.

127 and chemokine signaling, nucleotide-binding oligomerization domain-like receptor signaling and Janus

128 Nucleotide oligomerization domain-like receptor X1 (NLRX1) has been

129 TLR, nucleotide binding oligomerization domain-like receptor, and retinoic acid-

130 or components of the TLR, nucleotide binding oligomerization domain-like receptor, and retinoic acid-

131 matory processes, the nucleotide-binding and oligomerization domain-like receptor, leucine-rich repea

132 unity receptors, known as nucleotide-binding oligomerization domain-like receptors (NLRs), to recogni

133 present crystal structures of the MARV VP35 oligomerization domain.

134 re we present two crystal structures of this oligomerization domain.

135 utant, WT-holoenzyme, and a monomeric CaMKII oligomerization-domain deletion mutant control.

136 t evidence indicates that nucleotide-binding oligomerization domains (NODs) can also recognize a broa

137 ded within the human and fruitfly SMN YG-box oligomerization domains.

138 n the structure of the GabR effector-binding/oligomerization (Eb/O) domain suggest that binding a mon

139 Swi6 and Chp2 have similar dimerization and oligomerization equilibria, and that Swi6 binds slightly

140 Mutants that interfere with Nap1 oligomerization exhibit severe nucleosome assembly defec

141 n Abeta and inhibits its functions including oligomerization, fibrillation, and cytotoxicity.

142 Thus, we provide an approach to investigate oligomerization for arbitrary protein families leading t

143 ion path, most likely due to greater protein oligomerization from a minor structural change.

144 tabolic regulation and apoptosis, where VDAC oligomerization has been implicated with these processes

145 he Rev response element (RRE) and subsequent oligomerization in a cooperative manner.

146 , we demonstrate that the regulation of EHD2 oligomerization in a membrane-bound state is crucial to

147 of the traptamers with the EPOR induced EPOR oligomerization in an orientation that stimulated recept

148 into biomolecule patterning, clustering and oligomerization in biological systems.

149 transport within target cells, potential K28 oligomerization in the ER lumen is prevented by protein

150 While the exact role of oligomerization in the function of class A GPCRs such as

151 the RRE and Rev in vitro, and promoting Rev oligomerization in vitro.

152 studies demonstrate an essential role of FP oligomerization in vivo while our monomers enable detail

153 Mutation of a hydrophobic patch at the oligomerization interface decoupled peptide binding to h

154 embrane binding and also reveals a potential oligomerization interface in the C-terminal domain as we

155 the C-terminal domain as well as a conserved oligomerization interface in the mVP40 N-terminal domain

156 eratively promoting and directing gamma-TuSC oligomerization into MT nucleation-competent rings.

157 ical analyses of human CCL5 reveal that CCL5 oligomerization is a polymerization process in which CCL

158 ere nucleosome assembly defects showing that oligomerization is essential for the chaperone function.

159 We argue that ligand-induced oligomerization is essential to the regulation of EGFR s

160 While hSSB1 oligomerization is important for the removal of 8-oxogua

161 of the protein into oligomers and that SMSr oligomerization is promoted by curcumin, a drug known to

162 It is however unknown how LRRK2 oligomerization is regulated.

163 with the suggestion being that higher order oligomerization is required for its activation.

164 Oligomerization is triggered when polyphosphates bind to

165 measure the single-stranded DNA binding and oligomerization kinetics of wild-type and oligomerizatio

166 ligomeric macrocyclic depsipeptides using an oligomerization/macrocyclization process governed by a s

167 en configurations and use it to construct an oligomerization map that captures the paths of easy inte

168 The comparison of the two oligomerization maps highlights several key differences

169 t hDAT might function as a multimer, and its oligomerization may be relevant to addictive drug effect

170 ivity and cytotoxicity, indicating that ExoU oligomerization may have functional significance.

171 We suggest that oligomerization may promote pore enlargement.

172 edge, for (19)F solid-state NMR distance and oligomerization measurements by centerband-only detectio

173 The same oligomerization mechanism applies to the CD27L endolysin

174 ctive role of the IF consensus motifs in the oligomerization mechanism of tetramers during ULF format

175 he modeling reveals that these two competing oligomerization mechanisms play distinct roles: polymeri

176 o different larval gut proteins facilitating oligomerization, membrane insertion and pore formation.

177 potential significance because more complex oligomerization might lead to differences in substrate s

178 -helices on each side, representing a unique oligomerization mode among GBPs.

179 The compound did not affect heat-induced oligomerization, nuclear localization and specific DNA b

180 on of nucleoprotein-core links nucleoprotein oligomerization, nucleocapsid condensation, RNA encapsid

181 2 into the membrane, where G-domain-mediated oligomerization occurs.

182 Co-oligomerization of 1 and its germanium analogue gives a

183 Here, we show that oligomerization of a homologous bacterial Roco protein d

184 Non-enzymatic oligomerization of activated ribonucleotides leads to ri

185 uncover the importance of G4 recognition and oligomerization of AID in CSR.

186 Furthermore, the effect of lipid membrane on oligomerization of alpha-Syn is also investigated and th

187 Formed by oxidative oligomerization of catecholic small molecules, the physi

188 The helical domain is crucial for the oligomerization of CgT.

189 Oligomerization of Cox15 appears to be important for the

190 ed with lack of specific binding and reduced oligomerization of Cry1Ac in BBMV from NO-QAGE.

191 Oligomerization of defensins has been linked to their an

192 demonstrated that PI(4,5)P2 also induces the oligomerization of ExoU and that this PI(4,5)P2-mediated

193 results indicate that PI(4,5)P2 induces the oligomerization of ExoU, which may be a mechanism by whi

194 a mechanism that drives PI(4,5)P2 dependent oligomerization of FGF2.

195 erization of membrane-anchored FZD4 CRDs and oligomerization of full-length FZD4, which requires the

196 Both domains were required for GAG-dependent oligomerization of full-length MCK-2.

197 or, we confirmed that EVT901 interferes with oligomerization of full-length p75 neurotrophin receptor

198 Importantly, impairing oligomerization of hIRE1alpha LD abolished IRE1's activi

199 ding factor; rather, its binding promoted de-oligomerization of Hsp27, likely by competing for the se

200 We show that oligomerization of HsRAD51 leads to stepwise, but stocha

201 inding influences specificity, activity, and oligomerization of human RR, we aligned >300 eukaryotic

202 bonding and hydrophobic interactions in the oligomerization of IAPP-derived peptides.

203 with a parallel study showing that covalent oligomerization of ILEI is essential for EMT and tumor p

204 C-terminal tail region of IN in higher order oligomerization of intasomes, potentially informing futu

205 the ER membrane to the nucleus by promoting oligomerization of IRE1, a conserved transmembrane ER st

206 that this pair of side chains could promote oligomerization of kalata B1 through electrostatic inter

207 lex recruitment to centromeres by regulating oligomerization of M18BP1 through the Mis18alpha:Mis18be

208 Oligomerization of membrane proteins is common in nature

209 SLC25A46 results in increased stability and oligomerization of MFN1 and MFN2 on mitochondria, promot

210 Different effects of L-arginine on oligomerization of NAGS may have implications for effort

211 l insights into approaches for examining the oligomerization of neurotransmitter transporters and she

212 However, oligomerization of peroxisomal ABCD transporters is inco

213 Homo-oligomerization of proteins is abundant in nature, and i

214 These data suggest that oligomerization of RBA1 is required for function.

215 of RHD3 in the ER and can also facilitate an oligomerization of RHD3.

216 It has previously been suggested that the oligomerization of SNARE complexes required for cooperat

217 Antibody-induced oligomerization of sP-selectin or sP-selectin-Fc was req

218 Interestingly, Bbp1 induced oligomerization of Spc29, which may represent an early s

219 s stabilized by a supramolecular, tetrameric oligomerization of the Ce horizontal lineO units with ru

220 ite sequence (first TMSOTf then Et3N) led to oligomerization of the cinnamyl SF5- and CF3-acetates.

221 bind GAGs and are critical for GAG-dependent oligomerization of the full-length protein.

222 rt that this alternating array underlies the oligomerization of the GIPC/Myosin VI complexes in solut

223 ,3]-sigmatropic rearrangement and subsequent oligomerization of the intermediately formed cinnamyl es

224 Oligomerization of the long isoform of RTN3 is sufficien

225 ally, we applied these insights to study the oligomerization of the luminal domains of two nuclear me

226 ncluding IL-1beta and IL-18, by inducing the oligomerization of the multiprotein complex NLRP3-type i

227 cation site is formed by substrate-triggered oligomerization of the protein TatA.

228 and in vivo assays, we can show that higher oligomerization of the scTNF trimers results in more eff

229 This method is applied to the oligomerization of the tetramerization domain (TD) of th

230 n the membrane topology and disulfide-linked oligomerization of these two enzymes.

231 Oligomerization of transcription factors controls their

232 ation of F-actin and is also responsible for oligomerization of TRIOBP-1.

233 cREL, DeltaNp63alpha and TAp73 binding and oligomerization on NF-kappaB-, TP53- or AP-1-specific se

234 inding of DDX1 results in enhancement of Rev oligomerization on the RRE that is correlated with an RN

235 approach is suitable for mapping the impact oligomerization on transcription factor dynamics.

236 hese kinases may harbor regions that mediate oligomerization or control other aspects of signal trans

237 ns provide distinct contributions to Gag-Gag oligomerization, particle morphology, and biogenesis.

238 to provide distinct contributions to Gag-Gag oligomerization, particle morphology, and biogenesis.

239 he observed structural similarity and common oligomerization pathway between the two variants is like

240 ion with a membrane recruitment (FYVE) or an oligomerization (PB1) domain.

241 , C-O bond formation, hydrolysis of silanes, oligomerization, polymerization, metathesis, hydrosilyla

242 fication of a translational switch affecting oligomerization presented here has implications for the

243 ET efficiency-lifetime analysis to probe the oligomerization process of intrinsically disordered prot

244 at the A- and B-inserts distinctly alter the oligomerization propensity of Drp1 in solution as well a

245 We conclude that unique oligomerization properties of ClC-4 permit regulated tar

246 ation of these domains, coupled with dynamic oligomerization properties, is the basis for the remarka

247 using the blue light-sensitive dimerization/oligomerization property of A. thaliana Cryptochrome 2 (

248 of the protein, nor affects its stability or oligomerization property, however, it reduces the post-t

249 and CusC are connected to one another in an oligomerization ratio of 3:6:3 CusA/CusB/CusC to form th

250 The bicyclo-oligomerization reaction occurs through sequential acety

251 ty of both its hydrogen atom abstraction and oligomerization reactions can be attributed to its very

252 1 CA NTD/HTLV-1 CA CTD did not result in Gag oligomerization regardless of the parent Gag background.

253 tion significantly impaired effector-induced oligomerization required for enzyme activity, and oligom

254 high and CRY2low with elevated or suppressed oligomerization respectively, which we use to tune the l

255 antly, specific interference with ETO2-GLIS2 oligomerization reverses the transcriptional activation

256 the effects of the substitutions on peptide oligomerization, secondary structure dynamics, fibril as

257 ere, we tested the model by variation of the oligomerization state and by increase of the number of G

258 ests that physicochemical properties such as oligomerization state and DNA specificity, although tune

259 n secondary structures, or shared effects on oligomerization state and stability.

260 Because GR's oligomerization state has been implicated in therapy out

261 e available for researchers to determine the oligomerization state of membrane proteins in a static q

262 TuRC assembly is critically dependent on the oligomerization state of Spc110p, with higher-order olig

263 pending on the system composition and on the oligomerization state of the protein.

264 tor interactions are highly dependent on the oligomerization state of the receptor, and cellular fact

265 Strikingly, however, irrespective of the oligomerization state or presence of additional GABs, fi

266 Rather than changing the oligomerization state, heme induces a conformational cha

267 rupts the HA structure without affecting its oligomerization state.

268 progesterone receptors) reveals variation in oligomerization states among this family of transcriptio

269 dual alpha-SYN protein and assess its native oligomerization states from biological samples including

270 cability of this approach by quantifying the oligomerization states of membrane proteins tagged with

271 luorescent particle concentration and assess oligomerization states of proteins within defined region

272 nezumab and CreneFab can recognize different oligomerization states; however, the structural basis fo

273 ngation step with little effect on the early oligomerization steps in the lag time period.

274 rylated at serine 149, which regulates G3BP1 oligomerization, stress granule assembly, and RNase acti

275 ured linker region of Cox15 needed for Cox15 oligomerization, suggesting that this region mediates th

276 domain are key modulators of reversible Mfn oligomerization that drives fusion.

277 identify small-molecule inhibitors of STOML3 oligomerization that reversibly reduce the sensitivity o

278 dulation, allosteric regulation, and protein oligomerization, that control PTP activity.

279 he role of cholesterol in chemokine receptor oligomerization, thereby promoting the formation of a si

280 ch interferes with p75 neurotrophin receptor oligomerization through direct interaction with the firs

281 inutes, the information-rich 4D space (x, y, oligomerization, time) results were coupled to straightf

282 Y2-CIB1 interaction desire minimal CRY2 homo-oligomerization to avoid unintended complications, while

283 ded to other families of toxins that require oligomerization to exert toxicity.

284 f methane to methyl halides or their in situ oligomerization to higher hydrocarbons.

285 erved, and the presence of iron promoted its oligomerization up to six units.

286 ant, EphA2DeltaS-GFP, also underwent further oligomerization upon ephrinA1 stimulation, but the oligo

287 eover, Q282A eliminated cis-allostery in the oligomerization variant.

288 d introduce mutations to create low and high oligomerization versions.

289 merization required for enzyme activity, and oligomerization was rescued in the N291G/P294K enzyme.

290 classes of structurally related families is oligomerization, wherein a series of enzymatically catal

291 Akt phosphorylates TopBP1 and induces its oligomerization, which inhibits its ATR-activating funct

292 Gag protein is a primary determinant of Gag oligomerization, which is a critical step for immature G

293 responses and inflammatory diseases via self-oligomerization, which leads to the activation of the pr

294 from a fast to a slow binding state through oligomerization, which suggests that large A3G oligomers

295 eversal mutation of apposed residues reduces oligomerization while introduction of cysteines at these

296 ase domain, which mediates cycles of protein oligomerization with caRNAs, in response to ATP binding

297 ver, two C-terminal charges impact CRY2 homo-oligomerization, with positive charges facilitating olig

298 nergies for the analysis of membrane protein oligomerization within defined membranes.

299 that both XGh and XGo undergo fiber-to-fiber oligomerization without losing their crystallinity.

300 ed peptide binding to hIRE1alpha LD from its oligomerization, yet retained peptide-induced allosteric