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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 ciation of ARID1A with beta-catenin's folded Armadillo repeats.
5  directly bound polymerized vimentin via its 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 embly of dipeptide-specific modules based on armadillo repeats.
13  the positively charged groove formed by the armadillo repeats.
14 nal transactivation domain and the first two armadillo repeats.
15                      4.1R(+17b) binds to the armadillo repeats 1-2 of beta-catenin via its membrane-b
16 ic analysis reveals that PLSCR1 NLS binds to armadillo repeats 1-4 of importin alpha, but its interac
17    ICAT contains a 3-helix bundle that binds armadillo repeats 10-12 and a C-terminal tail that, simi
18 -terminal fragment of beta-catenin including armadillo repeats 10-12 binds to GAC63.
19 nd E-cadherin, binds in the groove formed by armadillo repeats 5-9 of beta-catenin.
20 served caspase consensus motif (DELD) within Armadillo repeat 6 of delta-catenin, was identified thro
21 for the difference in signaling and that the Armadillo repeats account for the remainder of the diffe
22 ficant functional domains: an amino-terminal armadillo repeat and an adjacent series of beta-catenin
23 e K(+) channel's alpha-subunit and the ninth armadillo repeat and carboxyl terminus of beta-catenin a
24 mino acid protein that contains 10 predicted Armadillo repeats and a C2 domain.
25 8p may bind the fusion machinery through its armadillo repeats and that palmitoylation brings this ma
26             Most importantly, SYS-1 bears 12 armadillo repeats and the SYS-1/POP-1 interface is ancho
27      The direct binding required most of the armadillo repeats and was mutually exclusive for interac
28 ne CG5155 encodes a protein that contains 10 Armadillo-repeats and has an unknown function.
29  from positions 133 to 363, which contains 4 armadillo repeats, and to the N-terminal adaptin-binding
30 1 (C311) in the noncatalytic, autoregulatory armadillo repeat (ARM) domain of SARM1.
31 or binding to the auto-inhibitory N-terminal armadillo repeat (ARM) domain of SARM1.
32    NMN binding triggers reorientation of the armadillo repeat (ARM) domains, which disrupts ARM:TIR i
33 -nucleosome interfaces, the ATPase-core ARID-armadillo repeat (ARM) module insertion site, the Arp mo
34                               ZIX encodes an Armadillo repeat (Arm) protein highly conserved across e
35                      We find that the entire armadillo repeat array of pendulin/Rch1 is necessary to
36                               The effects of armadillo repeat containing 5 (ARMC5) inactivation and o
37                                              Armadillo repeat containing 5 (ARMC5) is a cytosolic pro
38                   Human RBM48 interacts with armadillo repeat containing 7 (ARMC7).
39 otein product of the BHD gene, and p0071, an armadillo repeat containing protein that localizes to th
40 a coli universal stress protein); At3g54870 (armadillo-repeat containing kinesin-related protein); At
41 ggest that Gudu and ARMC4 are a subfamily of Armadillo-repeat containing proteins that may have an ev
42 ed proteomic screening approach, we identify armadillo repeat-containing 5 (ARMC5) as a CUL3 adaptor
43                Inactivating mutations in the Armadillo repeat-containing 5 (ARMC5) gene have recently
44 abidopsis (Arabidopsis thaliana) plant U box/armadillo repeat-containing E3 ligase9 (AtPUB9), we iden
45 ide polymorphism changing a splicing site in ARMADILLO REPEAT-CONTAINING KINESIN1.
46   Here we describe the identification of the armadillo repeat-containing protein, ARMCX3, as a Sox10-
47 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein
48 bling a protein kinase, termed STRAD, and an armadillo repeat-containing protein, named mouse protein
49 ins (Pkp-1, -2, and -3) comprise a family of armadillo repeat-containing proteins first identified as
50                             Plakophilins are armadillo repeat-containing proteins, initially identifi
51 ghly homologous to vertebrate ARMC4, also an Armadillo-repeat-containing protein enriched in testes,
52                                              Armadillo-repeat-containing proteins also exist in plant
53  of a complex between the PLSCR1 NLS and the armadillo repeat core of vertebrate importin alpha.
54 ive LXXLL peptide motifs in the beta-catenin armadillo repeats did not disrupt either binding to andr
55 meoDomain (residues Met442 to Trp495) and an ARMadillo repeat domain (residues Met566 to Glu862).
56 d a cluster of acidic residues in the second armadillo repeat domain and central linker domain of IP(
57 o a high-affinity pocket formed by the third armadillo repeat domain and linker domain promotes IP(3)
58 s containing the Pkp-3 head domain and Pkp-1 armadillo repeat domain localized to the desmosome and t
59   Previous yeast 2-hybrid screens, using the armadillo repeat domain of APC as bait, identified hTID-
60 by PKA promoted a tight association with the armadillo repeat domain of B-catenin at an extended regi
61 catenin-mediated transcription, bound to the armadillo repeat domain of beta-catenin, has been determ
62 ah-1 and TBL1 were found to bind to the same armadillo repeat domain of beta-catenin, suggesting that
63 complex between this region of Nup2p and the armadillo repeat domain of Kap60p.
64 he yeast two-hybrid system revealed that the armadillo repeat domain of p0071 bound directly to VE-ca
65 in and plakophilin-1 was not mediated by the armadillo repeat domain of plakophilin-1 but by the non-
66 terminal "tails" that flank the beta-catenin armadillo repeat domain on ligand binding have also been
67                              p120(ctn) is an Armadillo repeat domain protein with structural similari
68 rystal structure of the importin-alpha3/MOS6 armadillo repeat domain suggests that five of the six Ar
69 go proteins interact with the importin-alpha armadillo repeat domain via nuclear localization sequenc
70 s containing the Pkp-1 head domain and Pkp-3 armadillo repeat domain were localized to the nucleus in
71 lation of beta-catenin by CK2 is the central armadillo repeat domain, where carrier proteins like axi
72 n filaments, binds to beta-catenin's central Armadillo repeat domain.
73 ibed catenin which contains a more divergent Armadillo-repeat domain.
74                                          The armadillo repeat domains encoded by TTC12 and dopamine i
75 rminus of APC, involving both the heptad and armadillo repeat domains, whereas the APC binding site i
76       We identify a conserved class of U-box ARMADILLO repeat E3 ligases that are positive regulators
77                                      Stacked armadillo repeats, each consisting of 42 aa arranged in
78             delta-catenin is a member of the Armadillo repeat family and component of the adherens ju
79 ral, handle and helical domains, display the armadillo repeat fold.
80 ed a new catenin family member termed ARVCF (armadillo repeat gene deleted in VCFS) from the interval
81 e addressed the requirement and functions of armadillo repeat gene deleted in velo-cardio-facial synd
82 hree-dimensional structure of a beta-catenin armadillo repeat in complex with the liver receptor homo
83 eats that bear unexpected resemblance to the armadillo repeats in beta-catenin and the HEAT repeats i
84 localization results and the presence of the armadillo repeats in this protein, we suggest that the P
85 with diverse cellular functions also contain armadillo repeats including pendulin, Rch1, importin, SR
86 ge region of Armadillo, spanning six central Armadillo repeats, is required for DE-cadherin binding,
87      Here, we show that Arabidopsis thaliana ARMADILLO-REPEAT KINESIN1 (ARK1) plays a key role in roo
88   Here we report the identification of ARK1 (Armadillo-Repeat Kinesin1) via a genetic screen for enha
89 f a 42 amino acid sequence motif known as an armadillo repeat, mediates these interactions.
90 s of repeat-specific features, especially in armadillo repeat modules.
91  recently identified JBTS-associated protein armadillo repeat motif-containing 9 (ARMC9) in tandem-af
92 s a Thr653Lys substitution in the C-terminal armadillo repeat of beta-catenin and displayed a reduced
93 forms an alpha helix that binds to the first armadillo repeat of beta-catenin, which can be mutated t
94 mpetition experiments revealed that the 11th armadillo repeat of Vac8 is an important element for rec
95 es the groove formed by the third and fourth armadillo repeats of beta-catenin and thus precludes the
96                               The C-terminal armadillo repeats of beta-catenin may be an attractive t
97 e NH(2) terminus combined with the first six armadillo repeats of beta-catenin were shown to be neces
98 of XSox17 beta physically interacts with the Armadillo repeats of beta-catenin.
99    We further demonstrate that the T. gondii armadillo repeats-only protein (TgARO) mutant, which is
100    The structure shows a tandem array of ten armadillo repeats, organized in a right-handed superheli
101 -catenin binding with all other beta-catenin armadillo repeat partners.
102 s PF16, an axonemal protein containing eight armadillo repeats predicted to be important for flagella
103                                          The armadillo repeat protein ARVCF is a component of adheren
104 lamydomonas requires ARMC2/PF27, a conserved armadillo repeat protein associated with male infertilit
105 erin superfamily, the plakin family, and the armadillo repeat protein family.
106       We also show that the P. pastoris Vac8 armadillo repeat protein is not essential for macropexop
107 ae, Vac8p, a myristoylated and palmitoylated armadillo repeat protein, is required for homotypic vacu
108 rotein interaction assays, we found that the armadillo-repeat protein ARMH3 (C10orf76) binds to activ
109 , and ectopic expression, we have identified armadillo-repeat protein C10 (ArmC10) as a high-affinity
110                                              Armadillo repeat proteins (ArmRPs) recognize their targe
111                                     Designed armadillo repeat proteins (dArmRP) have been developed a
112 -specific binding protein, based on designed armadillo repeat proteins (dArmRP), binding to peptides
113                                      Natural armadillo repeat proteins (nArmRP) like importin-alpha o
114                This NLS is recognized by two armadillo repeat proteins (pendulin/Rch1/alpha-P1/hSrp1a
115  Plakoglobin and beta-catenin are homologous armadillo repeat proteins found in adherens junctions, w
116         The structural similarity of SNI1 to Armadillo repeat proteins implies that SNI1 may form a s
117 chanical unfolding pathway, the beta-catenin armadillo repeat region (ARM) displays low mechanostabil
118 gamma-catenin), p120(ctn) contains a central Armadillo repeat region by which it binds cadherin cytop
119 tant fragment of beta-catenin containing the armadillo repeat region has been determined.
120 catenin binding repeat from APC bound to the armadillo repeat region of beta-catenin.
121 terminal beta-catenin "tails" that flank the armadillo repeat region reduces the affinity for desmoso
122  gondii GAC and reveal a unique, supercoiled armadillo repeat region that adopts a closed ring confor
123 1) (PDZ) binding sites but lacks the central armadillo repeat region that binds cadherins and other p
124 ontaining protein (StBTB/POZ1) containing an Armadillo repeat region, was up-regulated in the mutant.
125 ive beta-catenin in the Wnt-on phase via the armadillo repeat region.
126                            We found that the armadillo-repeat region 6 to 9 (ARM6-9) of KAP3, require
127 ages a continuous core of amino-terminal Tim armadillo repeats, resembling how photolyases recognize
128 ), and sterile alpha motifs and beta-catenin/armadillo repeats (SARM).
129 five motifs similar to the so-called HEAT or armadillo repeats seen in the importins.
130 des approximately 200-kDa proteins with four Armadillo repeats similar to those in the nuclear pore p
131 eta-catenin, a family of proteins containing armadillo repeats, suggesting similar biological functio
132 -catenin is a mammalian brain protein in the Armadillo repeat superfamily with sequence similarity to
133  encodes a large conserved protein with HEAT/Armadillo repeats that functions with sax-1, an NDR cell
134 ain of beta-catenin but does not require the armadillo repeats, which mediate association with cadher
135 s protein and SPAG6 contain eight contiguous armadillo repeats, which place them in a family of prote
136 ystal structure of the PUL domain reveals an Armadillo repeat with high structural similarity to impo
137                     D-APC has seven complete armadillo repeats with 60% identity to its human homolog
138 eta-catenin physically interacts through its Armadillo repeats with the C-terminal transactivation do

 
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