ライフサイエンスコーパス: heteromultimer

1 mSTRPC4 therefore probably functions as a heteromultimer.

2 methylene ATP-sensitive receptor is a P2X2/3 heteromultimer.

3 t one form of VirB11 functions as a homo- or heteromultimer.

4 trate that TRPMLs interact to form homo- and heteromultimers.

5 dulation of heterologously expressed KCNQ2/3 heteromultimers.

6 nd whether they function as homomultimers or heteromultimers.

7 ting from the loss of expression of P2X(2/3) heteromultimers.

8 odulin, suggesting that functional CaCCs are heteromultimers.

9 d K+ channel subfamilies usually do not form heteromultimers.

10 TraR function, probably by forming inactive heteromultimers.

11 d by a combination of TRP homo- and TRP-TRPL heteromultimers.

12 er more abundant subunits into CaM kinase II heteromultimers.

13 d-gated cation channels, as homomultimers or heteromultimers.

14 as wvGIRK2 homomultimers or as GIRK1-wvGIRK2 heteromultimers.

15 th in heart and brain, appear to function as heteromultimers.

16 is the ability to link different sdAbs into heteromultimers.

17 Inclusion of Q2S in the heteromultimer also positively shifts the voltage depend

18 ry (CHO) cells expressing cloned Kv7.2 + 7.3 heteromultimers and AT1 receptors studied under perforat

19 DeltaBAFF can associate with BAFF in heteromultimers and diminish BAFF bioactivity and releas

20 data demonstrate that TRIM5 orthologues form heteromultimers and indicate that C-terminal extensions

21 The ability of these channels to form heteromultimers and interact with other ion channels und

22 NQ3, KCNQ4, and KCNQ5 homomultimers, KCNQ2/3 heteromultimers and native M current, but not currents f

23 forms were observed in leaves, two ISA1/ISA2 heteromultimers and one ISA1 homomultimer.

24 algamma1 forms functional channels only as a heteromultimer, and jShalgamma1 + jShal1 heteromultimers

25 s a heteromultimer, and jShalgamma1 + jShal1 heteromultimers are functional only in a 2:2 subunit sto

26 n HEK293T cells, they form homomultimers and heteromultimers, as shown by coimmunoprecipitation and i

27 option of increased component sdAbs in these heteromultimers by testing different sdAb heterohexamers

28 Smads form heteromultimers capable of contacting DNA through the am

29 yme of bacteriophage lambda, terminase, is a heteromultimer composed of a small subunit, gpNu1, and a

30 The epithelial sodium channel (ENaC) is a heteromultimer composed of three subunits, each having t

31 ltage-dependent calcium channels (VDCCs) are heteromultimers composed of a pore-forming alpha1 subuni

32 e, suggesting that GABAB receptors couple to heteromultimers composed of GIRK1 and GIRK2 channel subu

33 (BKi current), the BKi channels are largely heteromultimers composed of inactivation-competent subun

34 These channels are heteromultimers composed of Kir6.2 subunit, an inwardly

35 Native rod CNG channels are heteromultimers, composed of three CNGA1 subunits and on

36 tation properties of individual subunits and heteromultimers comprised of multiple subunits.

37 Rs), activated by glycine and glutamate, are heteromultimers comprised of NR1 and NR2 subunits.

38 photoresponse, indicating that TRPgamma-TRPL heteromultimers contribute to the photoresponse.

39 When coexpressed, Kv2.1 and Kv2.2 heteromultimers did not aggregate in somatodendritic clu

40 Our data indicate that heteromultimers do not form efficiently in an alpha-alph

41 ly active, we demonstrate that TRPL-TRPgamma heteromultimers form a regulated phospholipase C- (PLC-)

42 N-methyl-D-aspartate receptors (NMDARs) are heteromultimers formed by NR1 and NR2 subunits.

43 hat both the ISA1 homomultimer and ISA1/ISA2 heteromultimer function in the maize leaf.

44 to trans-complement despite forming a stable heteromultimer in vivo.

45 Ca(2+) (LRC) channels encoded by Orai1/Orai3 heteromultimers in vascular smooth muscle cells (VSMCs).

46 We investigated whether Shaker and eag form heteromultimers in Xenopus laevis oocytes using electrop

47 hat Shaker and eag do not coassemble to form heteromultimers in Xenopus oocytes.

48 ontrast to other species where the ISA1/ISA2 heteromultimer is the only active form.

49 the ability of the subunits to assemble into heteromultimers is highly variable.

50 in two translational start codons encoding a heteromultimer of approximately 160 to 170 kDa and havin

51 The receptor is a heteromultimer of core subunits, NR1, and one or more re

52 atrial G protein-regulated ion channel, is a heteromultimer of GIRK1 and CIR.

53 packaging enzyme of bacteriophage chi, is a heteromultimer of gpNul (21 kDa) and gpA (74 kDa) subuni

54 otein-coupled inwardly rectifying potassium (heteromultimer of KIR3.1 and KIR3.4) channels.

55 ized KATP is the pancreatic KATP which is an heteromultimer of Kir6.2 and SUR1 protein subunits.

56 ed by energy-harvesting complexes, which are heteromultimers of cytoplasmic membrane proteins with ho

57 ted and basally active Na+ currents, whereas heteromultimers of GIRK2 weaver and GIRK1 appeared to ha

58 KATP channels are heteromultimers of KIR6.2 and a sulfonylurea receptor, S

59 ium (KATP) channels in striated myocytes are heteromultimers of KIR6.2, a weak potassium inward recti

60 These channels are heteromultimers of sulfonylurea receptor (SUR) and KIR6.

61 ive potassium channels (K(ATP) channels) are heteromultimers of sulfonylurea receptors (SUR) and inwa

62 The K(1/2) values for heteromultimers of the alpha subunit and a chimeric beta

63 tial of mRNA therapeutics encoding long sdAb heteromultimers, one heterohexamer was encoded as replic

64 ection of Q2S with either Q2L, Q3, or Q2L/Q3 heteromultimers results in attenuation of K(+) current,

65 Studies of mutant GIRK1/GIRK4 heteromultimers reveal that the GIRK1 and GIRK4 subunits

66 cise MS analysis of the intact four-chain Ab heteromultimer reveals nonspecific, non-enzymatic reacti

67 ASIC2a homomultimeric channels nor ASIC1a/2a heteromultimers showed H(+)-activated [Ca(2+)](c) elevat

68 n and synaptophysin are present in homo- and heteromultimers, suggesting that a large fraction of the

69 lypeptide in the dynactin complex, a protein heteromultimer that binds to and may mediate the microtu

70 horylate adjacent subunits in the Kv channel heteromultimer that lack proline-rich SH3 domain ligand

71 ifferent Ca2+-binding affinities can lead to heteromultimers that can regulate the efficiency of exci

72 ABP and GRIP also form homo- and heteromultimers through PDZ-PDZ interactions but do not

73 two or more DEG/ENaC subunits coassemble as heteromultimers to generate transient H(+)-gated current

74 HeT-A and TART Gags form homo- and heteromultimers using a region containing major homology

75 To probe whether Kv2 isotypes can form heteromultimers, we developed a dominant-negative mutant

76 f Kv7.2-Kv7.4 homomultimers and of Kv7.2/7.3 heteromultimers were found to be strongly dependent on t

77 They also interact to form heteromultimers, which allows for a hybrid stimulatory a

78 kely to be mediated by Kv1.5-containing homo/heteromultimers, while I(Kv2) involves a Kv2.1 alpha-sub

79 related channel subunit, TRP-like, to form a heteromultimer with conductance characteristics distinct

80 form either a homomultimer with Kvbeta2 or a heteromultimer with Kvbeta1.

81 BEC3F in various human tissues and it formed heteromultimers with APOBEC3F or APOBEC3G in the cell.

82 Box or the C-terminal B30.2/SPRY domain form heteromultimers with full-length huTRIM5alpha and are do

83 eric Orai1 channels; however, Orai1 can form heteromultimers with its homolog, Orai3.

84 y, neuropilin-1 can homomultimerize and form heteromultimers with neuropilin-2.

85 ant over TraR, suggesting that they can form heteromultimers with the wild-type activator.

86 rlR inhibits conjugation by forming inactive heteromultimers with TraR.

87 re expressed in photoreceptor cells and form heteromultimers with TRP and with each other.