ライフサイエンスコーパス: homodimer

1 iana NFU1 assembles one [4Fe-4S] cluster per homodimer.

2 identified as ligands for the CD8alphaalpha homodimer.

3 PiSFI3 forms an unusual trans-homodimer.

4 ld type, and that there are two active sites/homodimer.

5 mediated through production of the IL-12p40 homodimer.

6 is functionally equivalent to the mouse MafA homodimer.

7 for many years that LPL was only active as a homodimer.

8 lly on the metabotropic glutamate receptor 2 homodimer.

9 eric Cdc10 drives assembly of the core Cdc10 homodimer.

10 monomer interacts with a monomer of the Cmu1 homodimer.

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

12 o comprehensively characterize the hole-hole homodimer.

13 nd 2-fold higher than the Ser(838)-harboring homodimer.

14 QC division depends on formation of the SHR homodimer.

15 ed for the stability and function of the TM2 homodimer.

16 microtubules over micrometer distances as a homodimer.

17 riptional program and DNA-damage repair as a homodimer.

18 BD2) bound to an RNA duplex as an asymmetric homodimer.

19 oloenzyme is a tetramer that consists of two homodimers.

20 ytoplasm, while none of these mutants formed homodimers.

21 no acid residue for the formation of HLA-B27 homodimers.

22 nic phospholipids, regulating activated PDK1 homodimers.

23 homodimers fourfold compared to constitutive homodimers.

24 lotypes (HLA-B*27:02 to HLA-B*27:09) to form homodimers.

25 ively formed antiparallel L18W-PGLa and MG2a homodimers.

26 d reduction in the lateral mobility of ErbB3 homodimers.

27 icans and Candida parapsilosis formed stable homodimers.

28 family of galectins and bridging potency of homodimers.

29 tudy the asymmetric function of melanocortin homodimers.

30 ient cells, MNT binds to MLX, but also forms homodimers.

31 ponsible for its compromised ability to form homodimers.

32 ponsible for its compromised ability to form homodimers.

33 -4 heterodimers being more stable than ClC-4 homodimers.

34 g heterodimers with bHLH TFs or from forming homodimers.

35 otility on single microtubules as individual homodimers.

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

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

38 sine 7 upon engagement by antibodies or KACL homodimers.

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

40 a transcriptional coregulator of p52 and p50 homodimers.

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

42 purify without contaminating GDF9 and BMP15 homodimers.

43 ers of BTB proteins while sparing functional homodimers.

44 2DeltaEx16) that forms constitutively active homodimers.

45 g affinity for NRXNs or its capacity to form homodimers.

46 nductance compared with the TRESK and TREK-2 homodimers.

47 nels are assembled as primitive antiparallel homodimers.

48 y rates of the KIF3AA and much slower KIF3CC homodimers.

49 chemical and motile properties as engineered homodimers.

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

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

52 chical equations of motion approach on model homodimers, a method used in the intermediate coupling r

53 ate T cells via an anti-CD3 (aCD3) arm, aCD3 homodimer (aCD3 HD) and high-molecular-weight species (H

54 ution within the hCCS interface reduces hCCS homodimer affinity, creating a pool of hCCS available to

55 nal dynamics of the two subunits forming the homodimer and allosteric perturbations on cGMP binding.

56 ent transcription factor, FgSR, that forms a homodimer and binds to a 16-bp cis-element of its target

57 emonstrated with holo glutaredoxin 5 (GLRX5) homodimer and holo GLRX5:BolA-like protein 3 (BOLA3) het

58 ACMSD forms a homodimer and is functionally inactive as a monomer beca

59 , while SSRV1 has a nucleocapsid formed by a homodimer and is not enveloped.

60 es as a switch to boost the activity of MDM2 homodimer and promote its self-destruction to enable rap

61 '3'-cGAMP induces closing of the human STING homodimer and release of the STING C-terminal tail, whic

62 ng of the spike trimer to more than one ACE2 homodimer and suggests a mechanical contribution of the

63 lete extracellular protocadherin-15 parallel homodimer and the tip-link bond.

64 his mutation eliminates the function of BMP7 homodimers and all other BMPs that normally heterodimeri

65 inetics of KIF3A and KIF3C when expressed as homodimers and analyzed in vitro are distinctively diffe

66 pting BRAF-containing dimers, including BRAF homodimers and BRAF-CRAF heterodimers, but not CRAF homo

67 y, we compared the immunogenicity of DENV2 E homodimers and DENV2 E monomers.

68 rbB3 and ErbB2 led to the formation of ErbB3 homodimers and ErbB3/ErbB2 heterodimers in a competitive

69 ia, the fastest variants discovered here are homodimers and exhibit a much simpler folding and activa

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

71 Furthermore, we found that GGA1t formed homodimers and heterodimers with GGA1.

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

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

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

75 enhancement of viral infectivity require Nef homodimers and support a mechanism by which the Nef dime

76 und that results in the stabilization of Max homodimers and the attenuation of Myc.

77 disease-associated HLA-B27 allotypes to form homodimers and the failure of HLA-B*27:03 to form homodi

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

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

80 tion of HER2 through disruption of HER2-HER2 homodimers, and (ii) the subsequent degradation of HER2

81 characteristics of KIF3C when expressed as a homodimer are exceeding slow, whereas homodimeric KIF3AA

82 Here we demonstrate that Nef homodimers are important for SERINC5 down-regulation, tr

83 mechanistic details of Syk docking on gamma homodimers are unresolved.

84 s, suggesting that RAF heterodimers, and not homodimers, are the major players in determining the amp

85 he insertion of one [4Fe-4S](2+) cluster per homodimer as determined by UV-visible absorption/CD, res

86 FtsZ-binding pocket, which defines the SepF homodimer as the functional unit, and suggests a reversi

87 K95 abrogates RNR activity by disrupting its homodimer assembly.

88 The two beta-subunits make a tightly bound homodimer at the center, and two alpha-subunits are boun

89 ssays, we show that both Lu and Lu(v13) form homodimers at the cell surface of epithelial cancer cell

90 in this motif coordinate a zinc ion in mZIP4 homodimers at the plasma membrane.

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

92 m that the two fluorophores in a Venus(A206) homodimer behave as a single-photon emitter.

93 sx2 binding represses transcription, whereas homodimer binding stimulates gene expression.

94 nature of this motif induces symmetric MITF homodimer binding.

95 dimers, suggesting a 1:1 (antibody:myostatin homodimer) binding stoichiometry.

96 We further show that a stable BST2 homodimer binds to ILT7, but post-binding events associa

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

98 As a homodimer, Bmh1 binds simultaneously to H3S10ph and the

99 wo different multidrug ABC transporters, the homodimer BmrA from Bacillus subtilis and the heterodime

100 plex shows Periphilin forms an alpha-helical homodimer, bound by a single TASOR molecule.

101 Bax1 exists in monomer or homodimer but forms a heterodimer exclusively with XPB.

102 hances the ubiquitin ligase activity of MDM2 homodimer but not MDM2-MDMX heterodimer.

103 mmetric surface pockets present on the PNPOx homodimer, but this site has never been verified by othe

104 The stabilized DENV2 homodimers, but not monomers, were efficiently recognize

105 Following stimulation by ATP, the NLRP6 homodimer can further assemble into a linear molecular p

106 s RAF function in normal cells in which CRAF homodimers can drive signaling.

107 imers and the failure of HLA-B*27:03 to form homodimers challenge the role of HLA-B27 homodimers in A

108 PRK is an elongated homodimer characterized by a large central beta-sheet of

109 owed a significantly reduced ability to form homodimers compared with all other allotypes, including

110 study of the full-length protein, revealed a homodimer comprising a coiled coil with two independent

111 xibility translates into an ensemble of ACE2 homodimer conformations that could sterically accommodat

112 athway perturbs equilibrium between the PDK1 homodimer conformations.

113 photosynthetic cytochrome b (6) f complex, a homodimer containing eight distinct subunits and 26 tran

114 ion of drug candidates, with minimal risk of homodimer contamination using a single Protein A chromat

115 Ste2 was purified as a homodimer coupled to two G proteins.

116 parallel beta-sheets assemble with symmetric homodimer cross sections.

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

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

119 in absence of PRO and incapable of forming a homodimer due to a steric clash of an ENZ-specific tyros

120 a small fraction was present as constitutive homodimers exhibiting a ~40% lower mobility than monomer

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

122 oteins: FemX adds the first glycine, and the homodimers FemA and FemB sequentially add two Gly-Gly di

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

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

125 oop in the carboxyl terminus of LPL prevents homodimer formation and forces LPL into a monomeric stat

126 c homology and Bcr homology domains disrupts homodimer formation and impacts PI3K signalling.

127 ), and Phe(121)) and demonstrated attenuated homodimer formation in a cell-based fluorescence complem

128 induce activation, supporting a role for Nef homodimer formation in the activation mechanism.

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

130 ted interswitch residues, thereby permitting homodimer formation.

131 s, in the areas for CD4 binding and putative homodimer formation.

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

133 Chd(T) forms a "head-to-tail" homodimer, formed between two alpha-helices from each mo

134 B3 significantly and reduced the mobility of homodimers fourfold compared to constitutive homodimers.

135 suggest piston-type TM signaling by the TM2 homodimer from PASP across the full TM region, whereas t

136 Here, we report that the CD8alphaalpha homodimer functions as a coreceptor for KIR3DL1, an inhi

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

138 ating desired bispecific molecules, parental homodimers, half molecules, and antibodies with mispaire

139 72, Thr76, Gly80' and Tyr83') forms a stable homodimer, has catalytic activity similar to the wild ty

140 sid proteins (from four heterodimers and two homodimers) have obvious structural homology while seque

141 These channels form homodimers; however, a few examples of heterodimerizatio

142 5D2-bound LPL monomers are as stable as LPL homodimers (i.e., they are not more prone to unfolding),

143 the complex differs from previously reported homodimer identified by X-ray crystallography.

144 MPE is a monomer, whereas Mre11 and SbcD are homodimers; (ii) MPE lacks the capping domain present in

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

146 roved sensitivity in detecting low-abundance homodimer impurities (LOD from 0.01% to 0.1%).

147 The chromatographic separation between homodimer impurities and bsAb, as achieved by the mmSEC

148 owever, sensitive detection of low-abundance homodimer impurities can still be challenging for regula

149 hnique in both detection and quantitation of homodimer impurities in bsAb samples.

150 ghly sensitive detection and quantitation of homodimer impurities in bsAb samples.

151 Detection and quantitation of homodimer impurities in therapeutic bispecific antibody

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

153 a 3.7 angstrom cryo-EM structure of the KimA homodimer in an inward-occluded, trans-inhibited conform

154 stance of the membrane and forms a stable TM homodimer in both the inactive and fumarate-activated st

155 hic studies demonstrated that RABL3 formed a homodimer in solution via interactions between the effec

156 AR wild type (WT) was expressed as a homodimer in the cytoplasm, while none of these mutants

157 to Pro767 and lead to dissociation of the AR homodimer in the cytoplasm.

158 revealing that full-length CYP102A1 forms a homodimer in which both the heme and FAD domains contact

159 orm homodimers challenge the role of HLA-B27 homodimers in AS pathoetiology.

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

161 BMP7/BMP4 heterodimers are more active than homodimers in vitro, but it is not known whether these h

162 on of TLR2/TLR1 heterodimers as well as TLR2 homodimers in vitro.

163 urified and were each shown to assemble into homodimers in water in the programmed way.

164 at the cross-linking time of alpha-actinin-4 homodimers increases approximately twofold within the ce

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

166 l structure of the EMC that consists of Erh1 homodimers interacting with Mmi1 in a 2:2 stoichiometry

167 Previous studies indicated that a HapX homodimer interacts with the CCAAT-binding complex (CBC)

168 s the third anchors a structural site at the homodimer interface.

169 ese ANGPTLs inactivate LPL by converting LPL homodimers into monomers, rendering them highly suscepti

170 LPL, does not require the conversion of LPL homodimers into monomers.

171 domain)/IR(intracellular-domain) demonstrate homodimer IRalpha enhances insulin binding and signaling

172 The hole-hole homodimer is an undesired variant generated during the p

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

174 Cryo-EM revealed that the Delta12 variant homodimer is conformationally more stable and incapable

175 usively on CD8(+) T cells, the CD8alphaalpha homodimer is present in subsets of T cells and human nat

176 we show that overexpression of a forced E2A homodimer is sufficient to drive robust neural commitmen

177 The function of CD8alphaalpha homodimers is largely unknown.

178 bility of the Escherichia coli beta-clamp, a homodimer, is particularly remarkable.

179 es that HLA-B27 heavy chains aberrantly form homodimers, is a central hypothesis that attempts to exp

180 single-molecule velocities of the engineered homodimers KIF3AA and KIF3CC are 293 and 7.5 nm/s, respe

181 eq and gene-editing we show that the p50/p50 homodimer known to act as repressor for a number of pro-

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

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

184 PKG1 exists as a parallel homodimer linked by an N-terminal leucine zipper, and we

185 Tobramycin homodimer may allow the use of lower doses of novobiocin

186 Pharmacological disruption of Nef homodimers may control HIV-1 infectivity and viral sprea

187 in speeds similar to KIF3AC, suggesting the homodimers mechanically impact each other's motility to

188 A FraB homodimer model generated by RosettaCM was used to build

189 D reconstruction of individual IgG hole-hole homodimer molecules.

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

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

192 Each component monomer of the Top2 homodimer nicks one of the DNA strands and forms a coval

193 eterodimer that corresponds to the canonical homodimer observed in all previously reported PRMTs.

194 loop, T-cell receptor binding, formation of homodimer of alpha-beta heterodimers, and cholesterol bi

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

196 9- angstrom resolution, depicting a parallel homodimer of protocadherin-15 EC1-3 molecules forming an

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

198 In VSMC, deleting IGF1R increases homodimers of IR, enhances insulin binding, stimulates p

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

200 We have previously shown evidence of stable homodimers of SERCA2a in heterologous cells and cardiomy

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

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

203 A binding specificity by forming cooperative homodimers on precisely spaced and oriented DNA sites.

204 interact with each other to form short-lived homodimers on the plasma membrane.

205 nd structural results indicate that the EutD homodimer opens the pyrimidine ring of ectoine through a

206 action of Omomyc is to bind DNA as either a homodimer or a heterodimer with Max that is formed cotra

207 DGAT1 can exist as either a homodimer or a homotetramer and the two forms have simil

208 ne helix while still not disrupting the ACE2 homodimer or ACE2-RBD interfaces.

209 n, which is expressed as 2 forms, alphaalpha homodimer or alphabeta heterodimer.

210 t AFF4-CHD mediates the formation of an AFF4 homodimer or an AFF1-AFF4 heterodimer.

211 MUR4 forms either a homodimer or heterodimers with its isoforms.

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

213 ers and BRAF-CRAF heterodimers, but not CRAF homodimers or ARAF-containing dimers.

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

215 two conserved binding modes: forming C2A/C2A homodimers, or forming a heterodimer with the zinc finge

216 as binding regulatory elements as monomers, homodimers, or heterodimers.

217 p40:p19), the p40 monomer (p40), and the p40 homodimer (p40(2)).

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

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

220 vation that only a single subunit of the p66 homodimer precursor is susceptible to HIV-1 protease.

221 Furthermore, the p66 homodimer precursor undergoes a conformational change in

222 by HIV-1 protease forms a 66 kDa chain (p66) homodimer precursor.

223 In the crystal structure of the AR LBD homodimer, Pro767 and Phe765 reside closely on a loop th

224 subunit of the periplasmic domain of the Tsr homodimer (pTsr) has an intact serine-binding site.

225 Although both growth factors exist as homodimers, recent evidence indicates that GDF9 and BMP1

226 nteractions between pMHC-I and CD8alphaalpha homodimers regulate KIR3DL1(+) NK cell education.

227 Of note, MNT-MNT homodimers regulated the transcription of some genes inv

228 ligand binding domain (LBD) of the mGluR7/7 homodimer revealed it to have an apparent affinity ~4000

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

230 zation of receptor complexes, including Ror2 homodimers, Ror2/Fzd7 and Ror2/dsh heterodimers in an en

231 crystal revealed a typical four-helix bundle homodimer, similar to previously well-studied chemorecep

232 ys revealed that Gsx2 binds both monomer and homodimer sites in the developing mouse ventral telencep

233 ncer containing a combination of monomer and homodimer sites.

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

235 the versatility of this method in separating homodimer species from bsAb based on either electrostati

236 (>=95%) by inducing partial disorder in one homodimer species without affecting the heterodimer.

237 ting the conformational dynamics of multiple homodimer states.

238 rinsic tryptophan for UV-B perception with a homodimer structure containing 26 structural tryptophan

239 rmacophore designed to target a melanocortin homodimer such that one receptor is occupied by an agoni

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

241 e prodomain in the pro- and latent myostatin homodimers, suggesting a 1:1 (antibody:myostatin homodim

242 eudomonas fluorescens can self-assemble into homodimer, tetramer, and higher-order structures.

243 ation of a more symmetrically arranged PD-L1 homodimer than that previously reported for other inhibi

244 unique 3(10)-helical feature present in MDM2 homodimer that allows pS429 to stabilize the closed E2-u

245 ering, and electron microscopy unveil an XPG homodimer that binds, unstacks, and sculpts duplex DNA a

246 In contrast, isolated FANCD2 is a homodimer that is unable to bind DNA, suggestive of an a

247 nd purified SaOhyA and found that it forms a homodimer that requires FAD for activity.

248 Golgins are thought to form extended homodimers that are C-terminally anchored to Golgi membr

249 ere, we produce stable recombinant E protein homodimers that are recognized by strongly neutralizing

250 tor allosteric signaling that occurs between homodimers that can be applied straightforwardly in vitr

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

252 structure epitopes present on Zika E protein homodimers that cover the surface of the virus.

253 y characterized bacterial beta-etherases are homodimers that fall into two distinct GST subclasses: L

254 ve form of E. coli Ia RNR is composed of two homodimers that form the active alpha(2)beta(2) complex.

255 peroxide H(2) Both COX isoforms are sequence homodimers that function as conformational heterodimers

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

257 d balance disorders and assemble as parallel homodimers that interact to form the tip link.

258 CADs are homodimers, the active center is located in the interfac

259 estigate heterodimerization among known GPCR homodimers: the CXC chemokine receptor 4 and sphingosine

260 The homodimer theory, which proposes that HLA-B27 heavy chai

261 DGAT1 forms a homodimer through N-terminal segments and a hydrophobic

262 The SH3 domain tends to generate homodimers through a domain swap.

263 We show that ING5 forms homodimers through its N-terminal domain, which folds in

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

265 Fascetto (Feo) in Drosophila, which forms a homodimer to cross-link interzonal MTs, ensuring proper

266 se findings, we test a model showing how the homodimer to monomer site ratio and the Gsx protein leve

267 Binding of semaphorin homodimer to plexin brings two plexins in close proximit

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

269 ite ligand-protein surface that engages BCL6 homodimers to form a supramolecular structure.

270 Additionally, RRM3 forms homodimers to increase its RNA binding affinity.

271 The heterodimer was also more resistant than homodimers to inhibition by RD3.

272 and in the vigorous activation of PDGFR-beta homodimers to produce CDRs.

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

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

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

276 ious studies have established that the Hsp90 homodimer undergoes an ATP-driven cycle through open and

277 e spatial domain organization within the p66 homodimer using pulsed Q-band double electron-electron r

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

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

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

281 S-box TF usually works by forming hetero- or homodimers, we conducted yeast-two-hybrid screening and

282 because ATF4 is unable to form highly-stable homodimers, we hypothesized that ATF4 may promote muscle

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

284 GAFb) and a catalytic domain, cone PDE6 is a homodimer whereas rod PDE6 consists of two homologous ca

285 pharmacological profile similar to the TRESK homodimer, whereas the presence of the TREK-2 subunit re

286 main' RXLR effector that forms a novel trans-homodimer which is required for its ability to suppress

287 ull-length OsCYP20-2 promotes OsFSD2 forming homodimers which enhance its activity, eliminating the a

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

289 ERp44 also forms Zn(2+)-bridged homodimers, which dissociate upon client binding.

290 erodimers are 10 times more stable than IAPP homodimers, which explains the substoichiometric ability

291 demonstrating that the CC3 forms a parallel homodimer whose dimer interface is formed by a small num

292 We found that (Pl)EctA forms a homodimer whose enzyme activity is highly regiospecific

293 t of their structures to form an intertwined homodimer, whose subunits resemble the monomer.

294 ein from methane-oxidizing bacteria, forms a homodimer with a dicopper Cu(A) center at the dimer inte

295 XtOTOP3 forms a homodimer with each subunit containing 12 transmembrane

296 RNase J1 is a homodimer with exonuclease activity aided by two metal c

297 the modern tetramer evolved-a noncooperative homodimer with high oxygen affinity that existed before

298 TSs are homodimers with active sites separated by ~30 angstrom.

299 a subset of kinesin-14 motors that exist as homodimers with an N-terminal microtubule-binding tail,

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