ライフサイエンスコーパス: heteropentameric

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 f agonist and do not necessitate the complex heteropentameric architecture of the modern-day protein.

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

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

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

11 GABA(A) receptors are heteropentameric channels comprised from subunits derive

12 The heteropentameric clamp loaders are circular oligomers, r

13 The adult GlyR is a heteropentameric complex composed of alpha1 and beta sub

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

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

16 at loop extrusion requires the assembly of a heteropentameric complex consisting of the SMC1/SMC3 het

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

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

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

20 Retromer is a heteropentameric complex that plays a specialized role i

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

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

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

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

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

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

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

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

29 urally, GABRP homopentamers closely resemble heteropentameric GABA(A)R anion channels, transitioning

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

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

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

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

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

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

36 eIF2B is the heteropentameric guanine nucleotide exchange factor that

37 eIF2B is a heteropentameric guanine-nucleotide exchange factor esse

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

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

40 Most GABA(A)Rs of the CNS are heteropentameric ion channels composed of two alpha, two

41 dult muscle-type acetylcholine receptors are heteropentameric ion channels formed from four different

42 dult muscle-type acetylcholine receptors are heteropentameric ion channels formed from two alpha-subu

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

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

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

46 Heteropentameric neuronal nicotinic receptors assemble s

47 n, and subunit interactions at the two major heteropentameric nicotinic receptors-those governing nic

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

49 Moreover, the heteropentameric receptor constituted by Phh-GRD1/Phh-LC

50 Here, we show that the heteropentameric Scar/Wave Regulatory Complex (WRC), whi

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

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