ライフサイエンスコーパス: armadillo repeat

1 tant of beta-catenin that lacks the internal armadillo repeats.

2 contains a coiled coil domain and 10 tandem armadillo repeats.

3 e that the protein contains eight contiguous armadillo repeats.

4 directly bound polymerized vimentin via its armadillo repeats.

5 embly of dipeptide-specific modules based on armadillo repeats.

6 02-512 of APC, a region including 2 of the 7 armadillo repeats.

7 a protein of unknown function that contains armadillo repeats.

8 ditionally contains leucine-rich repeats and Armadillo repeats.

9 c domain that binds directly to beta-catenin Armadillo repeats.

10 s inhibitory domains (DIDs) composed of five armadillo repeats.

11 sactivation domain, and (3) retention of the armadillo repeats.

12 the positively charged groove formed by the armadillo repeats.

13 nal transactivation domain and the first two armadillo repeats.

14 ic analysis reveals that PLSCR1 NLS binds to armadillo repeats 1-4 of importin alpha, but its interac

15 ICAT contains a 3-helix bundle that binds armadillo repeats 10-12 and a C-terminal tail that, simi

16 -terminal fragment of beta-catenin including armadillo repeats 10-12 binds to GAC63.

17 nd E-cadherin, binds in the groove formed by armadillo repeats 5-9 of beta-catenin.

18 served caspase consensus motif (DELD) within Armadillo repeat 6 of delta-catenin, was identified thro

19 for the difference in signaling and that the Armadillo repeats account for the remainder of the diffe

20 ficant functional domains: an amino-terminal armadillo repeat and an adjacent series of beta-catenin

21 e K(+) channel's alpha-subunit and the ninth armadillo repeat and carboxyl terminus of beta-catenin a

22 mino acid protein that contains 10 predicted Armadillo repeats and a C2 domain.

23 8p may bind the fusion machinery through its armadillo repeats and that palmitoylation brings this ma

24 Most importantly, SYS-1 bears 12 armadillo repeats and the SYS-1/POP-1 interface is ancho

25 The direct binding required most of the armadillo repeats and was mutually exclusive for interac

26 ne CG5155 encodes a protein that contains 10 Armadillo-repeats and has an unknown function.

27 from positions 133 to 363, which contains 4 armadillo repeats, and to the N-terminal adaptin-binding

28 ZIX encodes an Armadillo repeat (Arm) protein highly conserved across e

29 We find that the entire armadillo repeat array of pendulin/Rch1 is necessary to

30 The effects of armadillo repeat containing 5 (ARMC5) inactivation and o

31 Armadillo repeat containing 5 (ARMC5) is a cytosolic pro

32 otein product of the BHD gene, and p0071, an armadillo repeat containing protein that localizes to th

33 a coli universal stress protein); At3g54870 (armadillo-repeat containing kinesin-related protein); At

34 ggest that Gudu and ARMC4 are a subfamily of Armadillo-repeat containing proteins that may have an ev

35 Inactivating mutations in the Armadillo repeat-containing 5 (ARMC5) gene have recently

36 abidopsis (Arabidopsis thaliana) plant U box/armadillo repeat-containing E3 ligase9 (AtPUB9), we iden

37 ide polymorphism changing a splicing site in ARMADILLO REPEAT-CONTAINING KINESIN1.

38 Here we describe the identification of the armadillo repeat-containing protein, ARMCX3, as a Sox10-

39 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein

40 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein

41 ins (Pkp-1, -2, and -3) comprise a family of armadillo repeat-containing proteins first identified as

42 Plakophilins are armadillo repeat-containing proteins, initially identifi

43 ghly homologous to vertebrate ARMC4, also an Armadillo-repeat-containing protein enriched in testes,

44 Armadillo-repeat-containing proteins also exist in plant

45 of a complex between the PLSCR1 NLS and the armadillo repeat core of vertebrate importin alpha.

46 ive LXXLL peptide motifs in the beta-catenin armadillo repeats did not disrupt either binding to andr

47 s containing the Pkp-3 head domain and Pkp-1 armadillo repeat domain localized to the desmosome and t

48 Previous yeast 2-hybrid screens, using the armadillo repeat domain of APC as bait, identified hTID-

49 catenin-mediated transcription, bound to the armadillo repeat domain of beta-catenin, has been determ

50 ah-1 and TBL1 were found to bind to the same armadillo repeat domain of beta-catenin, suggesting that

51 complex between this region of Nup2p and the armadillo repeat domain of Kap60p.

52 he yeast two-hybrid system revealed that the armadillo repeat domain of p0071 bound directly to VE-ca

53 in and plakophilin-1 was not mediated by the armadillo repeat domain of plakophilin-1 but by the non-

54 terminal "tails" that flank the beta-catenin armadillo repeat domain on ligand binding have also been

55 p120(ctn) is an Armadillo repeat domain protein with structural similari

56 rystal structure of the importin-alpha3/MOS6 armadillo repeat domain suggests that five of the six Ar

57 go proteins interact with the importin-alpha armadillo repeat domain via nuclear localization sequenc

58 s containing the Pkp-1 head domain and Pkp-3 armadillo repeat domain were localized to the nucleus in

59 lation of beta-catenin by CK2 is the central armadillo repeat domain, where carrier proteins like axi

60 n filaments, binds to beta-catenin's central Armadillo repeat domain.

61 ibed catenin which contains a more divergent Armadillo-repeat domain.

62 The armadillo repeat domains encoded by TTC12 and dopamine i

63 rminus of APC, involving both the heptad and armadillo repeat domains, whereas the APC binding site i

64 We identify a conserved class of U-box ARMADILLO repeat E3 ligases that are positive regulators

65 Stacked armadillo repeats, each consisting of 42 aa arranged in

66 delta-catenin is a member of the Armadillo repeat family and component of the adherens ju

67 ral, handle and helical domains, display the armadillo repeat fold.

68 ed a new catenin family member termed ARVCF (armadillo repeat gene deleted in VCFS) from the interval

69 e addressed the requirement and functions of armadillo repeat gene deleted in velo-cardio-facial synd

70 hree-dimensional structure of a beta-catenin armadillo repeat in complex with the liver receptor homo

71 eats that bear unexpected resemblance to the armadillo repeats in beta-catenin and the HEAT repeats i

72 localization results and the presence of the armadillo repeats in this protein, we suggest that the P

73 with diverse cellular functions also contain armadillo repeats including pendulin, Rch1, importin, SR

74 ge region of Armadillo, spanning six central Armadillo repeats, is required for DE-cadherin binding,

75 Here, we show that Arabidopsis thaliana ARMADILLO-REPEAT KINESIN1 (ARK1) plays a key role in roo

76 f a 42 amino acid sequence motif known as an armadillo repeat, mediates these interactions.

77 s of repeat-specific features, especially in armadillo repeat modules.

78 s a Thr653Lys substitution in the C-terminal armadillo repeat of beta-catenin and displayed a reduced

79 forms an alpha helix that binds to the first armadillo repeat of beta-catenin, which can be mutated t

80 mpetition experiments revealed that the 11th armadillo repeat of Vac8 is an important element for rec

81 es the groove formed by the third and fourth armadillo repeats of beta-catenin and thus precludes the

82 The C-terminal armadillo repeats of beta-catenin may be an attractive t

83 e NH(2) terminus combined with the first six armadillo repeats of beta-catenin were shown to be neces

84 of XSox17 beta physically interacts with the Armadillo repeats of beta-catenin.

85 We further demonstrate that the T. gondii armadillo repeats-only protein (TgARO) mutant, which is

86 The structure shows a tandem array of ten armadillo repeats, organized in a right-handed superheli

87 -catenin binding with all other beta-catenin armadillo repeat partners.

88 s PF16, an axonemal protein containing eight armadillo repeats predicted to be important for flagella

89 The armadillo repeat protein ARVCF is a component of adheren

90 erin superfamily, the plakin family, and the armadillo repeat protein family.

91 We also show that the P. pastoris Vac8 armadillo repeat protein is not essential for macropexop

92 ae, Vac8p, a myristoylated and palmitoylated armadillo repeat protein, is required for homotypic vacu

93 Armadillo repeat proteins (ArmRPs) recognize their targe

94 -specific binding protein, based on designed armadillo repeat proteins (dArmRP), binding to peptides

95 Natural armadillo repeat proteins (nArmRP) like importin-alpha o

96 This NLS is recognized by two armadillo repeat proteins (pendulin/Rch1/alpha-P1/hSrp1a

97 Plakoglobin and beta-catenin are homologous armadillo repeat proteins found in adherens junctions, w

98 The structural similarity of SNI1 to Armadillo repeat proteins implies that SNI1 may form a s

99 chanical unfolding pathway, the beta-catenin armadillo repeat region (ARM) displays low mechanostabil

100 gamma-catenin), p120(ctn) contains a central Armadillo repeat region by which it binds cadherin cytop

101 tant fragment of beta-catenin containing the armadillo repeat region has been determined.

102 catenin binding repeat from APC bound to the armadillo repeat region of beta-catenin.

103 terminal beta-catenin "tails" that flank the armadillo repeat region reduces the affinity for desmoso

104 1) (PDZ) binding sites but lacks the central armadillo repeat region that binds cadherins and other p

105 ontaining protein (StBTB/POZ1) containing an Armadillo repeat region, was up-regulated in the mutant.

106 ive beta-catenin in the Wnt-on phase via the armadillo repeat region.

107 ), and sterile alpha motifs and beta-catenin/armadillo repeats (SARM).

108 five motifs similar to the so-called HEAT or armadillo repeats seen in the importins.

109 des approximately 200-kDa proteins with four Armadillo repeats similar to those in the nuclear pore p

110 eta-catenin, a family of proteins containing armadillo repeats, suggesting similar biological functio

111 -catenin is a mammalian brain protein in the Armadillo repeat superfamily with sequence similarity to

112 encodes a large conserved protein with HEAT/Armadillo repeats that functions with sax-1, an NDR cell

113 ain of beta-catenin but does not require the armadillo repeats, which mediate association with cadher

114 s protein and SPAG6 contain eight contiguous armadillo repeats, which place them in a family of prote

115 ystal structure of the PUL domain reveals an Armadillo repeat with high structural similarity to impo

116 D-APC has seven complete armadillo repeats with 60% identity to its human homolog

117 eta-catenin physically interacts through its Armadillo repeats with the C-terminal transactivation do