ライフサイエンスコーパス: homodimer

1 d symmetry that unexpectedly mimics the FabH homodimer.

2 ston displacements in one subunit of the Tsr homodimer.

3 at creates a positively charged channel as a homodimer.

4 f-function mechanism affecting the calpain 3 homodimer.

5 opsis thaliana, AtTPC1, which functions as a homodimer.

6 H' domain unfolding behavior of the p66/p66' homodimer.

7 lding landscape of the mature HIV-1 protease homodimer.

8 lly on the metabotropic glutamate receptor 2 homodimer.

9 -KIAA0157 heterodimer and an inactive BRCC36 homodimer.

10 ing a hydrophobic groove that spans the Get3 homodimer.

11 ion binder) stabilizes the EGFR ligand-bound homodimer.

12 f which are properties of the alphaE-catenin homodimer.

13 w that MtRecD exists in solution as a stable homodimer.

14 if distinct from that bound by the C/EBPbeta homodimer.

15 TaTFP crystallized as homodimer.

16 for antiproliferative drugs, is an obligate homodimer.

17 d adjacent to the C-terminal regions of each homodimer.

18 at it comprises a TA protein bound to a Get3 homodimer.

19 econd linker promotes separation of the Plk4 homodimer.

20 eric Cdc10 drives assembly of the core Cdc10 homodimer.

21 o comprehensively characterize the hole-hole homodimer.

22 ntation assays as strongly as alphaE-catenin homodimer.

23 -4 heterodimers being more stable than ClC-4 homodimers.

24 association are strongly coupled in receptor homodimers.

25 ein kinase activity compared to Mst1 or Mst2 homodimers.

26 lent ligands to target melanocortin receptor homodimers.

27 es into trimeric and hexameric structures of homodimers.

28 s, FXIII-A2B2, and isolated FXIII-A2 and -B2 homodimers.

29 y was intermediate between TREK-1 and TREK-2 homodimers.

30 n and proteasome-mediated degradation of p50 homodimers.

31 used here should be generally applicable to homodimers.

32 eractions in the heterodimer than in the two homodimers.

33 ten through induced dimerization via LC8:LC8 homodimers.

34 s) that are typically thought to function as homodimers.

35 close proximity between two neighboring Bak homodimers.

36 usion suggesting a functional role for Sec22 homodimers.

37 -molecular-weight insulin oligomers and IAPP homodimers.

38 s long) integral membrane protein that forms homodimers.

39 s of BCl-3 that mediate interaction with p50 homodimers.

40 e CRP/FNR transcription family of allosteric homodimers.

41 s forms of RAF dimers including BRAF or CRAF homodimers.

42 of this protein, and the tetherin TMD forms homodimers.

43 sine 7 upon engagement by antibodies or KACL homodimers.

44 , followed by the assembly of inactive Pol I homodimers.

45 a transcriptional coregulator of p52 and p50 homodimers.

46 ow that Pnc1 co-import requires Gpd1 to form homodimers.

47 ms, including alpha-Pcdhs, which cannot form homodimers.

48 ed SERCA2a revealed that SERCA readily forms homodimers.

49 Although assumed to form exclusive homodimers, 16 possible heterodimeric mGluRs have been p

50 kcal/mol) exceeds that of the Naph(+*)(Naph) homodimer (17.8 kcal/mol).

51 we investigated the hypothesis that bursicon homodimers act in prophylactic immunity in insects, and

52 ion and secreted levels of the inhibin betaA homodimer, activin A.

53 ckle's ability to selectively inhibit Relish homodimer activity contributes to proper host immunity a

54 ly that both CCC-bound monomer and cytosolic homodimer alphaE-catenin are required for strong cell-ce

55 re of OmoMYC and show that it forms a stable homodimer and as such recognizes DNA in the same manner

56 rminal domain of Tsc1 (998-1,164 aa) forms a homodimer and binds to both protomers of the Hsp90 middl

57 istic ligand CITCO binds directly to the CAR homodimer and dissociates phosphorylated CAR into its mo

58 We show that NRBF2 is a homodimer and drives the dimerization of the larger PI3K

59 ly with both (44)RKNR(47) motifs in the CCL5 homodimer and engaged residues Arg-47 and -17 from both

60 o the structure and assembly of the p85alpha homodimer and suggests that this protein is a highly dyn

61 more, we show that Steap3 is functional as a homodimer and that it utilizes an intrasubunit electron

62 structure of the acyl-CoA oxidase 1 (ACOX-1) homodimer and the ACOX-2 homodimer bound to its substrat

63 d mutagenesis, we demonstrate that the Nbp35 homodimer and the Nbp35-Cfd1 heterodimer are ATPases, wh

64 nhibiting the assembly of the functional ODC homodimer and, most uniquely, by targeting ODC for ubiqu

65 Our findings show that PHOX2B forms homodimers and heterodimerizes weakly with mutated prote

66 tematically the thermodynamic stabilities of homodimers and heterodimers of kainate and AMPA receptor

67 In mammals, NF-kappaB factors can form homodimers and heterodimers to activate gene expression.

68 itro, CCRL2 was found to constitutively form homodimers and heterodimers with CXCR2, a main neutrophi

69 Because PHOX2B forms homodimers and heterodimers with its paralogue PHOX2A in

70 RTKs are believed to form both homodimers and heterodimers, and the different dimers ar

71 finding that scaffold proteins tend to form homodimers and heterodimers.

72 (kDa), multi-domain enzymes and function as homodimers and higher oligomers.

73 that BCL-3 makes extensive contacts with p50 homodimers and in particular with ankyrin repeats (ANK)

74 We show that NKp65 forms homodimers and is phosphorylated at the hemITAM-embedded

75 measure the dimerization constants of CEACAM homodimers and isothermal titration calorimetry to deter

76 We construct and study models of MST2 homodimers and MST2-RASSF SARAH heterodimers, and we ide

77 h other GPCRs; however, the existence of APJ homodimers and oligomers remains to be investigated.

78 uclear PRB forms a complex including JUN/JUN homodimers and P54(nrb)/Sin3A/HDAC to repress transcript

79 found that PiT1 and PiT2 form high-abundance homodimers and Pi-regulated low-abundance heterodimers.

80 We also mapped the contacts between Bak homodimers and the lipid bilayer based on EPR spectrosco

81 used to determine the affinity of parental (homodimer) and bispecific (heterodimer) interactions wit

82 tures revealed the canonical NS1 symmetrical homodimer, and RNA binding required conserved basic resi

83 rofile change was observed for the hole-hole homodimer, and the multiple HIC peaks were explored and

84 in-specific VHH heterodimers, as well as VHH homodimers, and characterized them for their ability neu

85 ammaA8, gammaB2, and gammaB7 revealing trans-homodimers, and of C-terminal ectodomain fragments from

86 K2P channels usually function as homodimers, and only a few examples of heteromerization

87 heterodimer are intermediate between the two homodimers, and the distinct load-dependent behavior is

88 d by their SARAH domains and is favored over homodimers, and these heterodimers have much-reduced pro

89 nal impact in P. aeruginosa, suggesting that homodimers are a physiologically relevant state.

90 EXD1 homodimers are inactive as a nuclease but function as an

91 compared with cells in which alphaE-catenin homodimers are present.

92 Homodimers are the most common type of protein assembly

93 external pH but, unlike their corresponding homodimers, are activated by both acidic and alkaline co

94 an GALT (hGALT) ternary complex, revealing a homodimer arrangement that contains a covalent uridylyla

95 d the structures of the C9923-55 monomer and homodimer as a function of membrane lipid composition us

96 R can bind to bZip domains of the C/EBPalpha homodimer as both a monomer and dimer of the DNA-binding

97 VioA forms a "loosely associated" homodimer as indicated by small-angle x-ray scattering e

98 structure-function relationship of caspase 8 homodimers as putative targets in cancer.

99 due to hydrogen bonding, especially to form homodimers as seen from X-ray data in the solid state.

100 HER2 forms homodimers as well as heterodimers with other HER family

101 ulum-plasma membrane contact sites therefore homodimer assembly may regulate Sec22 activity across a

102 ed accurate and reproducible quantitation of homodimers at the 0.2% (w/w) level, with the single-addi

103 valent to 1:1 mixtures of KIF3AA plus KIF3CC homodimers at the same motor concentration.

104 2m-free B27 heavy chain structures including homodimers (B272) can also be expressed at the cell surf

105 emain poorly characterized, as compared with homodimers, because of limitations in current experiment

106 The symmetrical apo hEXOG homodimer becomes asymmetrical upon binding to DNA, prov

107 ular domain of DSG2, thereby disrupting DSG2 homodimers between epithelial cells.

108 pose that previously described BH3-in-groove homodimers (BGH) are juxtaposed via the 'alpha3/alpha5'

109 ith a half-site motif is more prevalent than homodimer binding.

110 Recent data have shown that the DYNLT1 homodimer binds to two dynein intermediate chains to sub

111 An NlpI homodimer binds two molecules of Prc and forms three-sid

112 oxidase 1 (ACOX-1) homodimer and the ACOX-2 homodimer bound to its substrate.

113 COX-2 is a sequence homodimer, but the enzyme displays half-of-site reactivi

114 ere employed to "break the symmetry" of a Mb homodimer by pairing Mb constructs with complementary hi

115 that has been historically characterized as homodimer by X-ray crystallography.

116 rodimer has also been distinguished from the homodimers by its unique single channel conductance.

117 have demonstrated that the de novo design of homodimers can be achieved to atomic-level accuracy by b

118 rol proteins, i.e., the monomer CD86 and the homodimer CD28, and 2) relies on cell fixation to limit

119 forming the homodimer subunits, but the two homodimers coassemble in forming the heterotetramer.

120 The antitoxin protein CcdA is a homodimer composed of two monomers that each contain a f

121 , reported before, with each protomer in the homodimer comprising five domains.

122 ers exhibit equivalent activity to wild-type homodimers, consistent with half-of-the-sites reactivity

123 were markedly enhanced in beta1-adrenoceptor homodimers constrained by bimolecular fluorescence compl

124 o study, as it must form an obligate modular homodimer containing the PDZ proteins scribble and syntr

125 show that SMCHD1 forms an active GHKL-ATPase homodimer, contrasting with canonical SMC complexes, whi

126 Specifically, an ACOX-1 homodimer controls the production of ascarosides with si

127 s with seven or fewer carbons, and an ACOX-2 homodimer controls the production of those with omega-si

128 hat the DNA-binding preferences of AR and GR homodimers differ significantly, both within and outside

129 We report that these dsRBD homodimers display structural asymmetry and that this un

130 H2O2 induces a 50-kDa DJ-1 interprotein homodimer disulfide, known to form between Cys-53 on eac

131 e beta-catenin.cadherin complex, whereas the homodimer does not bind beta-catenin but interacts with

132 Further, the p85alpha homodimer enhances the lipid phosphatase activity and me

133 d1 heterodimer are ATPases, whereas the Cfd1 homodimer exhibited no or very low ATPase activity.

134 A solution NMR structure shows that the homodimer exhibits parallel helical packing similar to t

135 stabilization and refolding of the hole-hole homodimer Fc.

136 In addition to forming homodimers, FGF14 binds directly to the Nav1.6 channel C

137 molecule located at the center of the PD-L1 homodimer, filling a deep hydrophobic channel-like pocke

138 easurements, this FADA was evolved to form a homodimer for the activation of MG dyes.

139 preferential formation of heterodimers over homodimers for some members of the TGF-beta family.

140 Normally, ATM kinase is in an inactive, homodimer form and is transformed into monomers upon act

141 DBD T38D with CAR LBD, converting CAR to the homodimer form.

142 nsmembrane domain was required for efficient homodimer formation and for membrane fusion suggesting a

143 otein oxidation and impaired endothelial NOS homodimer formation as plausible mechanistic explanation

144 coordination of Fe-S clusters, whereas Glrx3 homodimer formation did not.

145 hydrophobic surface that facilitates initial homodimer formation.

146 masked CAR's dimer interface, preventing CAR homodimer formation.

147 ent insulin oligomers and compared with IAPP homodimer formation.

148 main-swapping region, strongly suggestive of homodimer formation.

149 tational method for the modeling of parallel homodimers formed by transmembrane (TM) alpha-helices.

150 While attempting to engineer a homodimer from a 51-amino-acid fragment of the monomeric

151 electively cross-link and down regulate HER2 homodimers from the plasma membranes of bulk cancer cell

152 nction mutant (which must function as an XLF homodimer) fully complements the c-NHEJ deficits of some

153 cles is experimentally revealed by comparing homodimer H-bond energies of aromatic heterocycles with

154 tions into just one protomer of a Y1/Y1 BiFC homodimer had no impact on efficient NPY-stimulated endo

155 modimers, in vivo Most covalent PilN or PilO homodimers had minimal functional impact in P. aeruginos

156 increased formation of dopamine receptor D2 homodimers has been suggested to be associated with the

157 72, Thr76, Gly80' and Tyr83') forms a stable homodimer, has catalytic activity similar to the wild ty

158 body-antigen interaction and heterodimer and homodimer heat shock protein complexes.

159 nd ligand-binding domain (LBD), enabling the homodimer-heterodimer conversion.

160 ay supports Gpd1 monomer import but not Gpd1 homodimer import and Pnc1 co-import.

161 electrophoresis revealed that CAR can form a homodimer in a configuration in which the PP2A/RACK1 bin

162 a model in which PLB interacts with a SERCA homodimer in a stoichiometry of 1:2.

163 uced the DNA-binding affinity of the p50-p50 homodimer in LPS-primed and -rechallenged macrophages, i

164 -based assays showed that CacyBP/SIP forms a homodimer in NB2a cell lysate, and biophysical methods d

165 e apoprotein, R-opsin, may indeed exist as a homodimer in rod disk membranes.

166 the FAD-binding domain to form a bell-shaped homodimer in solution with a maximal dimension of 110 A.

167 Rv2466c is a homodimer in which each subunit displays a modular archi

168 esults suggest that SERCA forms constitutive homodimers in live cells and that dimer formation is not

169 ncy in structures predicted for C99 congener homodimers in membrane and micelle environments.

170 ctor-kappaB1 (NF-kappaB1) and p52/NF-kappaB2 homodimers in nuclei where it modulates transcription in

171 SlRd2 was an ATP-binding protein that formed homodimers in planta.

172 tein sulfotransferases are known to exist as homodimers in the Golgi membranes, this organization lev

173 K heterodimers differ in function from TRAAK homodimers in two critical ways: they are activated by b

174 extended polymer, formed by archaeal histone homodimers, in a quasi-continuous superhelix with the sa

175 PilNO heterodimers, as well as PilN and PilO homodimers, in vivo Most covalent PilN or PilO homodimer

176 We infer the bursicon homodimers induce expression of AMP genes via Relish2 in

177 toplasmic domain of intact chemoreceptor Tar homodimers inserted into lipid bilayers of Nanodiscs.

178 B7-2 homodimer interface mimotopes prevent superantigen letha

179 fide bond between Cys-45 residues within the homodimer interface of Rgg2 from Streptococcus dysgalact

180 rantigens engage both B7-2 and CD28 at their homodimer interfaces, areas remote from where these core

181 aling can be controlled through the receptor homodimer interfaces.

182 ixture of donor-labeled and acceptor-labeled homodimers into heterodimers.

183 We thus deduce that the EC1-4 antiparallel homodimer is a general interaction strategy that evolved

184 The symmetry of a homodimer is broken in heterodimeric reaction-center str

185 been concluded that cytosolic alphaE-catenin homodimer is not important for intercellular adhesion be

186 to determine dissociation constants of c-Fos homodimers (Kd = 6.7 +/- 1.7 muM) and c-Fos-c-Jun hetero

187 y a lack of phosphorylation of the EPOR/EPOR homodimer, lack of activity in off-target selectivity sc

188 Treating larvae and adults with r-bursicon homodimers led to up-regulation of five anti-microbial p

189 components (c-Fos or Jun), bind STAT-1 in a homodimer like complex (HDLC).

190 zed at the PM, as opposed to their vesicular homodimer localization.

191 crease in the fraction/stability of the EGFR homodimer may have a significant biological impact on th

192 Covalent homodimers mediated by inter-Cys232 bonding alone are al

193 d Sdk2 ectodomain regions, revealing similar homodimers mediated by the four N-terminal immunoglobuli

194 Thus, the homodimer-monomer conversion is the underlying molecular

195 Here we demonstrate that CAR undergoes homodimer-monomer conversion to regulate this dephosphor

196 we found Nkx3-1 and Oct-transcription factor homodimer motifs to be enriched in TOT preferential bind

197 Here we show that, in addition to forming homodimers, Mst1 and Mst2 heterodimerize in cells, this

198 Once activated, how BAK homodimers multimerize to form the putative apoptotic po

199 The recently reported noncovalent homodimer (ncUbq) is expected to have greater conformati

200 l GCs mediate gene expression by favoring GR homodimer occupancy at classic palindromic sites at the

201 Ocr is a homodimer of 116 amino acids and adopts an elongated str

202 nd with Phe at 1.8 A resolution, revealing a homodimer of ACT folds with Phe bound at the dimer inter

203 meric association, consisting of a disc-like homodimer of CNNM2BAT bound to two independent PRL-1 mol

204 sent the structure of the antiparallel EC1-4 homodimer of human PcdhgammaB3, a member of the gamma su

205 biosynthesis of cladofulvin, an asymmetrical homodimer of nataloe-emodin produced by the fungus Clado

206 s the type-I IFN pathway upon binding to the homodimer of the adaptor protein STING on the surface of

207 The enzyme forms a homodimer of two 60-kDa subunits.

208 An active CPAF is a homodimer of two identical intramolecular heterodimers,

209 ingle molecule level, transient formation of homodimers of dopamine receptors in the membrane of stab

210 Homodimers of Etv1, Etv4, and Etv5 could be reduced to m

211 variants, including covalent and noncovalent homodimers of half antibodies (hAbs), may be present in

212 s formed from anti-electrostatic anion-anion homodimers of organophosphates and cyanostar macrocycles

213 a quaternary organization similar to that of homodimers of reoviruses and other dsRNA mycoviruses.

214 sed heterodimer stability as compared to the homodimers of their constituents, matching well physiolo

215 Here, we measured APJ monomer-homodimer-oligomer interconversion by monitoring APJ dyn

216 elish2 abolished the influence of r-bursicon homodimers on AMP production.

217 that can be converted to either the inactive homodimer or the active heterodimer.

218 RcsB regulates transcription either as a homodimer or together with auxiliary regulators, such as

219 tudies have demonstrated that CXCR4 can form homodimers or can heterodimerize with other G-protein-co

220 T2 either forms homodimers or heterodimerizes with T1 subunits that prov

221 ptor-alpha (RXRalpha) binds to DNA either as homodimers or heterodimers, but it also forms homotetram

222 on of human IgG, creating a fully functional homodimer (or "lysibody") with high-affinity binding and

223 ells produced greater levels of p40 than p40 homodimer (p402), IL-12, or IL-23.

224 ronment, leading to substantial variation in homodimer peptide structure as a function of membrane li

225 The resulting 2:2 complex of the bisulfate homodimer persists across all states of matter, includin

226 timal and often suffer from contamination by homodimers posing purification challenges.

227 subunit-specific processing of the p66/p66' homodimer precursor.

228 Insv homodimers preferentially bind CCAATTGG palindromes thro

229 e 2:2 heterotetramer comprises two different homodimers, rather than two heterodimers.

230 mediated through p35-p40 heterodimers or p40 homodimers, respectively.

231 DNA interactomes of 80 heterodimers and 22 homodimers revealed that 72% of heterodimer motifs corre

232 or both subunits of covalently linked mGluR2 homodimers reveals that receptor activation is highly co

233 FR heterodimers may be as significant as the homodimer roles.

234 or compounds with affinity for the caspase 8 homodimer's interface.

235 stic implications for the arrangement of the homodimer's N-terminal TOG domains during microtubule po

236 EPOR homodimers signal to promote the maturation of erythroid

237 d more strongly than either of the symmetric homodimers since DNA is a nearly symmetric target.

238 rse homo-oligomers in solution, and 15 (four homodimers, six homotrimers, six homotetramers and one h

239 s-based methods is challenging because these homodimer species and the bsAb often have similar physic

240 f oxidative modification on SOD1 monomer and homodimer stability, the key molecular properties relate

241 Here, we show that cooperativity and homodimer stabilization are strongly dependent on the pr

242 microscopy analysis demonstrates that SMCHD1 homodimers structurally resemble prokaryotic condensins.

243 We demonstrate that the C9923-55 homodimer structures form a heterogeneous ensemble with

244 The TCR zeta-chain is a homodimer subunit that contains six ITAMs (12 sites) and

245 the heterotetramer segregate in forming the homodimer subunits, but the two homodimers coassemble in

246 cted between RTA and the non-truncated P2-P2 homodimer, suggesting that the structural architecture o

247 phosphofructokinase-2 (Pfk-2) is an obligate homodimer that follows a highly cooperative three-state

248 ce, whereas cytosolic alphaE-catenin forms a homodimer that interacts more strongly with F-actin.

249 the nucleic acid, while the P domains form a homodimer that interacts with receptors.

250 ructural analyses indicate that Ccp1 forms a homodimer that is required for its anti-CENP-A loading a

251 main and forms a highly unusual antiparallel homodimer that is stably associated with MC2 receptors a

252 The YbiB protein is a homodimer that, therefore, has two electropositive DNA b

253 Like MinD, FlhG forms homodimers that are dependent on ATP and lipids.

254 ring actin-polymerizing factors, function as homodimers that bind with the barbed end of actin filame

255 sequence homology and form disulphide-linked homodimers that contain a pair of acidic aspartic acid r

256 tudies show that each bursicon subunit forms homodimers that induce prophylactic immunity in Drosophi

257 in a novel back-to-back orientation in both homodimers through Ig1:Ig2, Ig1:Ig1 and Ig3:Ig4 interact

258 d receptor (GR), which is known to bind as a homodimer to a palindromic DNA sequence.

259 he Escherichia coli chorismate mutase (EcCM) homodimer to be dependent on incorporation of a noncanon

260 The glucocorticoid receptor (GR) binds as a homodimer to genomic response elements, which have parti

261 Binding of a CsrA homodimer to the 5'UTR of an mRNA occludes the Shine-Dal

262 CAR undergoes a conversion from inactive homodimers to active heterodimers with retinoid X recept

263 igands with enhanced activity and can enable homodimers to signal in a context in which they normally

264 cer and activator of transcription 1 (Stat1) homodimers to Stat1-Stat2 heterodimers.

265 ocated in the dimer interface of the Ec-NhaA homodimer together with a beta-sheet.

266 Discovery of the PGL homodimer, together with previous results, suggests a mo

267 matted into scalable bsAbs that were free of homodimer traces by combining interface exchange, asymme

268 Compared with the hole-hole homodimer under different storage conditions, the bispec

269 inity, which places the DNA residence of the homodimers under thermodynamic rather than kinetic contr

270 nus autoinhibits Cdc3 association with Cdc10 homodimers until prior Cdc3-Cdc12 interaction.

271 cl-2 family, Bcl-xL is not converted to 3DDS homodimer upon binding BH3 peptides and ABT-737, a BH3 m

272 tion and reliable quantitation of these bsAb homodimers using liquid chromatography (LC) or capillary

273 s illustrated through the preparation of the homodimers UU-34 and TT-35 in 18 steps with an excellent

274 provided a better understanding of both the homodimer variant and the bispecific molecule.

275 ed interface of the reconstituted PsIAA4 PB1 homodimer variant, whose stoichiometry (1:1) and equilib

276 contribute to the relative bioactivities of homodimers versus heterodimers in vivo.

277 inding partners, BECN1 forms an antiparallel homodimer via its coiled-coil domain (CCD).

278 Rtt103 forms homodimers via its long coiled-coil domain and associate

279 The hole-hole homodimer was demonstrated to adopt a more homogeneous c

280 a/beta constant domain pair and the IgG1 CH3 homodimer was evidenced by X-ray crystallography and use

281 ble homodimers, whereas c-Fos leucine zipper homodimers were found to be much less stable in earlier

282 cular dynamics modeling confirmed that c-Fos homodimers were stably associated and could bind to the

283 is cycle but can still adopt a high-affinity homodimer when bound to a transition-state analog.

284 The NaARADL1 protein can form homodimers when transiently expressed in Nicotiana benth

285 cine zipper fragments could also form stable homodimers, whereas c-Fos leucine zipper homodimers were

286 the DeltaL1 TEAD DBD reveals a helix-swapped homodimer wherein helix 1 is swapped between monomers.

287 describe the structure of a PcdhgammaB7 cis-homodimer, which includes the membrane-proximal extracel

288 ction data derived a model of the PsIAA4 PB1 homodimer, which is comparable with other PB1 domain dim

289 ,5-bisphosphate (PIP2) only induces vinculin homodimers, which are asymmetric, we show that phospholi

290 n and proteasome-mediated degradation of p50 homodimers, which prolonged binding of NF-kappaB heterod

291 tylase dHDAC1, selectively repressing Relish homodimers while leaving other NF-kappaB dimer combinati

292 AtDPE1 forms a homodimer with a deep, long, and open-ended active site

293 H/gL, which exists predominantly as (gH/gL)2 homodimer with a molecular mass of 220 kDa in solution,

294 l characterization of a alpha-helix-mediated homodimer with C2 symmetry based on a monomeric Drosophi

295 KorA is a homodimer with the 101-amino acid subunits, folding into

296 vity for c-Myc-Max heterodimers over Max-Max homodimers with IC50 values as low as 5.6 muM.

297 the leptospiral PerR revealed an asymmetric homodimer, with one monomer displaying complete regulato

298 terface may drastically destabilize the SOD1 homodimer, with several modifications exhibiting a compa

299 The SusC transporters form homodimers, with each beta-barrel protomer tightly cappe

300 because GGDEF enzymes function as symmetric homodimers, with each monomer binding to one substrate N