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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.
10 l synthesis of sequence-defined, non-peptide heterooligomers.
11              ORMDL proteins formed homo- and heterooligomers and displayed similar patterns of intera
12                                 Formation of heterooligomers and similar interaction patterns with pr
13                    Phosphorylated Smads form heterooligomers and translocate into the nucleus where t
14 al protein complex systems (homooligomers, a heterooligomer, and a protein-ligand complex, ranging fr
15 ressed together, the two isoforms form large heterooligomers, and a small fraction of CaMKIIbeta is s
16  found that they form homooligomers, but not heterooligomers, and exhibit mutually exclusive binding
17 Z and AtpI, as homooligomers, and perhaps as heterooligomers, are Mg2+ transporter, Ca2+ transporter,
18    Our data suggest that a large gp78-Ube2g2 heterooligomer brings multiple Ube2g2 molecules into clo
19                                    Extending heterooligomer chain length beyond 12-15 residues minimi
20  monomers, Vpu homooligomers, and Vpu-target heterooligomers coexist, and suggests that the conserved
21 nd Cav1.3 proteins simultaneously, forming a heterooligomer complex.
22 r the mixed solution shows the presence of a heterooligomer composed of equal parts of Abeta40 and Ab
23                 Finally, we demonstrate that heterooligomers composed of NTD-fused proteins can be dr
24 at FtsH from Chlamydomonas reinhardtii forms heterooligomers comprising two subunits, FtsH1 and FtsH2
25 ta(21-30) co-assembled with Abeta(1-42) into heterooligomers containing mostly a single Abeta(1-42) a
26 TFs co-assembled with Abeta(1-42) into large heterooligomers containing multiple Abeta(1-42) and inhi
27                  A series of distinct BODIPY heterooligomers (dyads, triads, and tetrads) comprising
28                             The relevance of heterooligomer formation to spinal analgesic synergy req
29  knock-in mouse studies have shown that MDM2 heterooligomer formation with its homolog, MDMX, is nece
30 in interaction with betaA3-crystallin during heterooligomer formation, and the solubility of betaB1-c
31 allin interact with alphaA-crystallin during heterooligomer formation.
32 n its structural properties and stability of heterooligomers formed by wild-type (WT) betaB1 or its d
33 raction with Vpu, and that formation of each heterooligomer has a similar dissociation constant (Kd)
34                             The formation of heterooligomers has been proposed as a molecular basis f
35 e function and regulation of these homo- and heterooligomers in vivo remain incompletely understood.
36 alprotectin (CP; S100A8/S100A9 or MRP8/MRP14 heterooligomer) inhibits iron uptake and induces an iron
37  to characterize the energetics of homo- and heterooligomer interactions between the Vpu TMD and seve
38            Although forming a heterodimer or heterooligomer is essential for MDM2 and MDMX to fully c
39    Within the S100 family, the S100A8/S100A9 heterooligomer is essential for providing high-affinity
40 e-particle analysis by EM confirmed that the heterooligomer is octameric and revealed that the subuni
41               In eukaryotes, RNR comprises a heterooligomer of alpha(2) and beta(2) subunits.
42        In eukaryotes, the enzyme comprises a heterooligomer of alpha(2) and beta(2) subunits.
43         The thermal stability results of the heterooligomer of betaB1- plus betaA3-crystallins sugges
44                                Rat SP-A is a heterooligomer of two closely related isoforms, that req
45 egulation was reversible, and both homo- and heterooligomers of IP3Rs were equally susceptible to Ang
46 in plant leaves and assembles correctly into heterooligomers (pentamers and hexamers).
47 a-barrel assembly machine (BAM), a universal heterooligomer that contains a TamA homolog (BamA) and t
48 nalysis of this intermediate suggests that a heterooligomer that facilitates the membrane integration
49  proteins are secreted almost exclusively as heterooligomers that are defective in activating the com
50  Ca2+ channels are a large family of related heterooligomers that couple cell excitability to intrace
51  that neuropilin-1 and -2 can form homo- and heterooligomers through an interaction involving at leas
52 lope protein gp120IIIB to the CD4/CXCR4/CCR5 heterooligomer was negligible, and the gp120-induced cyt
53 re, CTRP9 and adiponectin can be secreted as heterooligomers when cotransfected into mammalian cells,
54 at ectopic ROR1 expression induced ROR1/ROR2 heterooligomers, which recruited GEFs, and enhanced prol
55  of betaB1-crystallin per se and that of the heterooligomer with betaA3-crystallin are dependent on t
56 idominance is consistent with PEX1 forming a heterooligomer with PEX6 that is poisoned by pex1-3 subu
57 54-61 homooligomers at 37 degrees C, forming heterooligomers with an intermediate mass of 625 kDa.
58  lacks a transactivation domain, it can form heterooligomers with full-length p53 and modulate the p5
59 e suggests that MDM2 forms homooligomers and heterooligomers with MDMX, the function and regulation o
60 rough a comparison of more than 30 different heterooligomers with mixed chiral and achiral side chain
61 rom unrelated subfamilies can associate into heterooligomers with novel signaling properties.