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1 ction involves preassembled BRI1-BAK1(SERK3) heterooligomers.
2 e fragments coassembled with Abeta42 to form heterooligomers.
3 ynaptic vesicle proteins that form homo- and heterooligomers.
4 mount of wild-type Pmp22 in heterodimers and heterooligomers.
5 gen bond donors and acceptors, form homo- or heterooligomers.
6 l by neuropilin-1 and -2, either as homo- or heterooligomers.
7 ant protein and the wild-type protein formed heterooligomers.
8 tion occurs in trans within envelope protein heterooligomers.
9 specific nucleic acid binding modes of these heterooligomers.
13 al protein complex systems (homooligomers, a heterooligomer, and a protein-ligand complex, ranging fr
14 ressed together, the two isoforms form large heterooligomers, and a small fraction of CaMKIIbeta is s
15 found that they form homooligomers, but not heterooligomers, and exhibit mutually exclusive binding
16 Z and AtpI, as homooligomers, and perhaps as heterooligomers, are Mg2+ transporter, Ca2+ transporter,
17 Our data suggest that a large gp78-Ube2g2 heterooligomer brings multiple Ube2g2 molecules into clo
19 monomers, Vpu homooligomers, and Vpu-target heterooligomers coexist, and suggests that the conserved
21 r the mixed solution shows the presence of a heterooligomer composed of equal parts of Abeta40 and Ab
22 at FtsH from Chlamydomonas reinhardtii forms heterooligomers comprising two subunits, FtsH1 and FtsH2
23 ta(21-30) co-assembled with Abeta(1-42) into heterooligomers containing mostly a single Abeta(1-42) a
24 TFs co-assembled with Abeta(1-42) into large heterooligomers containing multiple Abeta(1-42) and inhi
26 knock-in mouse studies have shown that MDM2 heterooligomer formation with its homolog, MDMX, is nece
27 in interaction with betaA3-crystallin during heterooligomer formation, and the solubility of betaB1-c
29 n its structural properties and stability of heterooligomers formed by wild-type (WT) betaB1 or its d
30 raction with Vpu, and that formation of each heterooligomer has a similar dissociation constant (Kd)
32 e function and regulation of these homo- and heterooligomers in vivo remain incompletely understood.
33 to characterize the energetics of homo- and heterooligomer interactions between the Vpu TMD and seve
35 Within the S100 family, the S100A8/S100A9 heterooligomer is essential for providing high-affinity
36 e-particle analysis by EM confirmed that the heterooligomer is octameric and revealed that the subuni
41 egulation was reversible, and both homo- and heterooligomers of IP3Rs were equally susceptible to Ang
43 nalysis of this intermediate suggests that a heterooligomer that facilitates the membrane integration
44 proteins are secreted almost exclusively as heterooligomers that are defective in activating the com
45 Ca2+ channels are a large family of related heterooligomers that couple cell excitability to intrace
46 that neuropilin-1 and -2 can form homo- and heterooligomers through an interaction involving at leas
47 lope protein gp120IIIB to the CD4/CXCR4/CCR5 heterooligomer was negligible, and the gp120-induced cyt
48 re, CTRP9 and adiponectin can be secreted as heterooligomers when cotransfected into mammalian cells,
49 at ectopic ROR1 expression induced ROR1/ROR2 heterooligomers, which recruited GEFs, and enhanced prol
50 of betaB1-crystallin per se and that of the heterooligomer with betaA3-crystallin are dependent on t
51 idominance is consistent with PEX1 forming a heterooligomer with PEX6 that is poisoned by pex1-3 subu
52 54-61 homooligomers at 37 degrees C, forming heterooligomers with an intermediate mass of 625 kDa.
53 e suggests that MDM2 forms homooligomers and heterooligomers with MDMX, the function and regulation o
54 rough a comparison of more than 30 different heterooligomers with mixed chiral and achiral side chain
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