ライフサイエンスコーパス: coassemble with

1 ortant aspects of effector secretion: (i) It coassembles with a second regulator (Pcr1) on the inner

2 suggested a mechanism by which the fragments coassembled with Abeta42 to form heterooligomers.

3 Alpha-internexin also coassembles with all three neurofilament proteins into a

4 Beta subunits are thought to coassemble with alpha subunits in a 1:1 stoichiometry, s

5 We conclude that the pi subunit coassembles with alpha, beta, and gamma subunits to form

6 Within the rat striatum, this subunit coassembles with alpha2, beta1, and gamma1, suggesting t

7 ed, indicating that Cav1.3 channels normally coassemble with alpha2delta2 at IHC presynapses.

8 defective in GTP binding and hydrolysis can coassemble with and stimulate GTP hydrolysis by wild-typ

9 CN1b, an integral subunit of Na(V) channels, coassembles with and modulates the biophysical propertie

10 rotrimer, [alpha1(V)]2alpha2(V), and it both coassembles with and regulates type I collagen-fibril di

11 We considered that K(V)LQT1 might coassemble with another subunit to form functional chann

12 Voltage-gated calcium channels can coassemble with auxiliary subunit alpha2delta isoforms 1

13 a7 subunits are coexpressed, colocalize, and coassemble with beta2 subunit(s).

14 The hybrid RHF Janus dendrimer coassembled with both RF and RH.

15 DCX coassembles with brain microtubules, and recombinant DCX

16 raphy experiments demonstrated that Caskin 1 coassembles with CASK on the immobilized cytoplasmic tai

17 ment of Cav2 channels in the brain, directly coassemble with Cav2.2 channels upon heterologous coexpr

18 ctenophore Shaker subfamily channel subunits coassembled with cnidarian and mouse Shaker subunits, bu

19 ith age in monkey prefrontal cortex, and can coassemble with delta subunits to form functional GABA(A

20 Although Kir6.1 or Kir6.2 coassemble with different SUR isoforms to form heteromul

21 heir role in Drp1 membrane recruitment, MiDs coassemble with Drp1 in vitro.

22 foci at mitochondrial constriction sites and coassemble with Drp1 to drive fission.

23 s, it is not known whether Kir6.1 and Kir6.2 coassemble with each other.

24 ests to determine whether these subunits can coassemble with each other.

25 ysiological evidence that the pi subunit can coassemble with either alpha5beta3 or alpha5beta3gamma3

26 y that beta-filagenin is a core protein that coassembles with either myosin or paramyosin in C. elega

27 sly introduced into hippocampal neurons, can coassemble with endogenous NR1 and NR2A and can reduce t

28 The chimeric GFP-NFH coassembled with endogenous neurofilaments.

29 , in which four channel-tethered RCK domains coassemble with four soluble (untethered) RCK domains.

30 When coassembled with FtsZ on lipid monolayers, these FtsA mi

31 ich synthesize Pol as a Gag-Pol protein that coassembles with Gag.

32 ays reduced binding to Gbetagamma and cannot coassemble with GIRK1.

33 GluClalpha2 coassembles with GluClbeta to form heteromeric channels

34 tors require two copies of the GluN1 subunit coassembled with GluN2 (and/or GluN3) subunits into a he

35 domain adopts a more open conformation when coassembled with GluN2A than with GluN2B.

36 mossy fiber synapses where they most likely coassemble with GluR6 subunits to form functional hetero

37 Gag proteins of endogenous retroviruses can coassemble with HIV-1 Gag and modulate the late phase of

38 Furthermore, HERV-K(CON) Gag was found to coassemble with HIV-1 Gag, as demonstrated by (i) proces

39 Multiple K(+) channel alpha-subunits that coassemble with Hk, including Shaker, Ether-a-go-go, and

40 Phospholipids were also coassembled with hybrid RHF Janus dendrimers.

41 KCNE1 encoding a transmembrane protein which coassembles with K+ channels mediating slow K+, I(Ks), c

42 to therapeutically target ion channels that coassemble with KCNE beta-subunits.

43 functionally distinct potassium channels by coassembling with KCNE ancillary subunits MinK and MiRP2

44 KCNQ1 alpha-subunits coassemble with KCNE1 beta-subunits to form channels tha

45 eart, KCNQ1 voltage-gated potassium channels coassemble with KCNE1 beta-subunits to generate the IKs

46 s from the colon, stomach, and kidney, KCNE3 coassembles with KCNQ1 to form K(+) channels that are vo

47 nificantly, we show that Kir2.6 subunits can coassemble with Kir2.1 and Kir2.2 in vitro and in vivo.

48 either Kvbeta1.2 or Kvbeta1.3, both of which coassemble with Kv1.5 and induce fast inactivation.

49 t that a splice variant of the Kv3.4 subunit coassembles with Kv3.1 subunits in rat brain FS neurons.

50 ng associated with channel inactivation when coassembled with KvLQT1.

51 In cocultures, alpha4(V) collagen coassembles with laminin on the surface of polarized Sch

52 ted double-ring structures that bind ATP and coassemble with LIP5/Vta1.

53 isoform does not by itself form OAPs but can coassemble with M23 in OAPs as heterotetramers.

54 rehybridized with a thiolated short DNA) was coassembled with mercaptohexanol onto the gold surface o

55 Merg1b coassembles with Merg1a to form channels with deactivati

56 MIIA(F46) coassembled with MIIB(alpha)(F47)-wt and -CK-5D and alte

57 A virus, referred to as a virophage, that is coassembled with Mimivirus in the host amoeba.

58 Therefore, K(V)LQT1 is the subunit that coassembles with minK to form I(Ks) channels and I(Ks) d

59 can also form slower activating channels by coassembling with MinK-related peptide 2 (MiRP2), a sing

60 nst a 70-kDa human ELP and showed that ELP70 coassembled with MTs in HeLa cell extracts and colocaliz

61 ypical rapid desensitization, and they could coassemble with native P2X2 subunits in pheochromocytoma

62 e-cell imaging data argue strongly that M18A coassembles with NM2 into mixed bipolar filaments.

63 Neto1 and Neto2 auxiliary subunits coassemble with NMDA receptors (NMDARs) and kainate rece

64 Here we show that NR3A coassembles with NR1-1a and NR2A to form a receptor comp

65 and the need for the synthesized proteins to coassemble with nuclear-encoded subunits have had substa

66 PARs) is observed when pore-forming subunits coassemble with or without auxiliary subunits, respectiv

67 ked inactivation, suggesting that Kv3.1b may coassemble with other members of the Kv3 subfamily.

68 ecific and isoform-redundant functions while coassembled with other NM II isoforms.

69 ed rectifier K+ channel Kv1.1 (Kv1.1N206Tag) coassembles with other K+ channels of the Kv1 subfamily

70 quitously expressed cytoplasmic protein that coassembles with pallidin and the muted protein in the B

71 he QD was used as a central nanoplatform and coassembled with peptides or oligonucleotides that were

72 that NF180 could not self-assemble but could coassemble with rat NFL, suggesting the existence of add

73 However, Cp-Y132A will coassemble with the wild-type protein on the basis of li

74 nvelope proteins (E1 or E2) were efficiently coassembled with the wild-type HBV S protein into subvir

75 In the colon, stomach, and kidney, KCNE3 coassembles with the alpha-subunit KCNQ1 to form K(+) ch

76 The KCNE1 auxiliary subunit coassembles with the Kv7.1 channel and modulates its pro

77 heart, has rapid deactivation kinetics, and coassembles with the longer isoform in Xenopus oocytes.

78 in division by specifically interacting and coassembling with the guanosine triphosphate-bound form

79 ostsynaptic density, however, AMPA receptors coassemble with transmembrane AMPA receptor regulatory p

80 eas irreversible binding results when tau is coassembled with tubulin into a tau-microtubule copolyme

81 in Xenopus laevis oocytes, two NR3 subunits coassemble with two NR1 subunits to form a glycine-gated

82 he intermediate filament (IF) protein nestin coassembles with vimentin and promotes the disassembly o

83 s a single-transmembrane domain protein that coassembles with voltage-gated K+ channel KVS-1 in the n

84 two-hybrid assay, since these same molecules coassemble with wild-type Gag into Ty1 virus-like partic

85 gnated dominant negative (DN), were found to coassemble with wild-type PA and generate defective hept

86 When expressed in trans, TubZ(D269A) coassembles with wild-type TubZ and significantly reduce