ライフサイエンスコーパス: heterooligomeric

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1 In the absence of a heterooligomeric adaptor complex composed of FCHO, Eps15

2 6-Phosphofructokinases (Pfk) are homo- and heterooligomeric, allosteric enzymes that catalyze one o

3 re illustrated by separating components from heterooligomeric assemblies formed between tetrameric tr

4 that cofactors and Torsins associate to form heterooligomeric assemblies with a defined Torsin-activa

5 initial signals for both homooligomeric and heterooligomeric assembly into receptors with GABAC prop

6 g Kvbeta subunits, our findings suggest that heterooligomeric assembly of these subunits occurs to in

7 he presence of an intermediate population of heterooligomeric channels consisting of Kvalpha1.2 with

8 related, mechanism(s); namely, "locking" the heterooligomeric channels in their closed state.

9 ant role(s) in modulation of the kinetics of heterooligomeric channels.

10 l point interact with BamA, a component of a heterooligomeric complex (Bam complex) that catalyzes OM

11 chemical analyses revealed that the PTP is a heterooligomeric complex composed of VDAC, SPG7, and Cyp

12 We analyzed the heterooligomeric complex of LmClpP1 and LmClpP2 via coex

13 al domain can function normally within the P heterooligomeric complex to carry out transcription and

14 light the functional importance of Mfn1-Mfn2 heterooligomeric complexes and the close interplay betwe

15 NMDA receptors are heterooligomeric complexes comprised of both NR1 and NR2

16 )beta subunits form multimolecular homo- and heterooligomeric complexes in human vascular smooth musc

17 fn1, but the functional significance of such heterooligomeric complexes is unknown.

18 with this hypothesis, Pop1p and Pop2p formed heterooligomeric complexes when overexpressed, and bindi

19 becomes the dominant HSF and is able to form heterooligomeric complexes with HSFA1.

20 SEP3 has been shown to form homo and heterooligomeric complexes with other MADS domain transc

21 lements mutant Mfn2 through the formation of heterooligomeric complexes, including complexes that for

22 proteins that assemble into symmetric linear heterooligomeric complexes, which in turn are able to po

23 on in vivo, notwithstanding the formation of heterooligomeric complexes.

24 nnels, kinetic properties of single homo and heterooligomeric ENaCs formed by the subunits with indiv

25 kinetic behavior of both homooligomeric and heterooligomeric ENaCs, although the carboxy-terminal do

26 sitizing component, even faster than that of heterooligomeric GABA(A) receptors, in striking contrast

27 hether the same region contained signals for heterooligomeric interaction with rho2 subunits.

28 netic resonance (EPR) to probe the homo- and heterooligomeric interactions of reconstituted sarcoplas

29 GABAA receptors are heterooligomeric ligand-gated anion channels that exhibi

30 americ module, eight of which form a single, heterooligomeric midplane ring, which is flexible in a d

31 vity in a heterogeneous protein mixture or a heterooligomeric protein (20), or determining if multipl

32 isolation, but together form a thermostable heterooligomeric Rca that can use both alpha-proteobacte

33 be regulated by factor-binding-induced homo/heterooligomeric restructuring, paving the way to cell m

34 The flagellum is a heterooligomeric structure that protrudes from the surfa

35 tive phenotype results from the formation of heterooligomeric VacA complexes with defective functiona

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