ライフサイエンスコーパス: heteropentameric

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1 e 5-HT3AB receptor is the best-characterized heteropentameric 5-HT3 receptor.

2 Clamp-loader complexes are heteropentameric AAA+ ATPases that load sliding clamps o

3 At the heart of the replicase machinery is a heteropentameric AAA+ clamp-loading machine that couples

4 Replication factor C (RFC) is a heteropentameric AAA+ protein clamp loader of the prolif

5 We find that both heteropentameric alpha3-containing receptors (alpha3*-nA

6 ent ligands- we show this to be the case for heteropentameric (alpha4beta2) and homopentameric (alpha

7 te that the functional ARC channel pore is a heteropentameric assembly of three Orai1 subunits and tw

8 ture, and their assembly is catalyzed by the heteropentameric Bam complex containing the outer membra

9 system and are driven in part by a class of heteropentameric beta2-containing nicotinic acetylcholin

10 The heteropentameric clamp loaders are circular oligomers, r

11 human checkpoint Rad proteins, we purified a heteropentameric complex composed of hRad17-RFCp36-RFCp3

12 The afRFC subunits form a heteropentameric complex consisting of one copy of the l

13 d trimeric PIX form an unusual high-affinity heteropentameric complex in which each Spa homology doma

14 Eukaryotic replication factor C (RF-C) is a heteropentameric complex that is required to load the re

15 Eukaryotic replication factor C is the heteropentameric complex that loads the replication clam

16 Similarly we found that hRad17 makes a heteropentameric complex with the four RFC small subunit

17 highly regulated by a genetically conserved heteropentameric complex, termed retromer.

18 They are found in heteropentameric complexes whose role in regulating WAVE

19 remodeling during mitosis is catalyzed by a heteropentameric enzyme known as condensin.

20 ition is primarily mediated by activation of heteropentameric GABA(A) receptor complexes.

21 lar localization and intrinsic properties of heteropentameric GABA(A) receptors themselves also const

22 The neurotransmitter GABA activates heteropentameric GABA(A) receptors, which are composed m

23 d alpha5 subunits) in the composition of the heteropentameric GABA(A)-R subunit assembly without a ch

24 lays an important role in forming the mature heteropentameric glycine receptors in these brain stem n

25 The isolated enzyme is a heteropentameric glycoprotein composed of two alpha-subu

26 obutyric acid type A (GABA(A)) receptors are heteropentameric glycoproteins.

27 Ligand-gated heteropentameric GlyRs form chloride ion channels that c

28 nslation initiation factor 2B (eIF2B) is the heteropentameric guanine nucleotide exchange factor for

29 eIF2B is the heteropentameric guanine nucleotide exchange factor that

30 ranslation initiation factor 2B (eIF2B) is a heteropentameric guanine nucleotide exchange factor that

31 eIF2B is a heteropentameric guanine-nucleotide exchange factor esse

32 tations in the alpha1-subunit (GLRA1) of the heteropentameric human inhibitory glycine receptor (hGly

33 ieu, suggesting that asymmetric occupancy of heteropentameric ion channels by alkylphenol-based anest

34 GABAARs are heteropentameric ligand-gated channels formed by the com

35 Members of the heteropentameric ligand-gated ion channel superfamily ra

36 als that it occurs not only in the classical heteropentameric "monomer" form, but that it also adopts

37 Heteropentameric neuronal nicotinic receptors assemble s

38 receptors in the central nervous system, are heteropentameric proteins assembled from distinct subuni

39 Models of the open state of the heteropentameric Torpedo nicotinic acetylcholine recepto

40 Here, we present the structure of a heteropentameric TRAPPI assembly complexed with Ypt1p.

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