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1 ments in the absence but not the presence of actin capping protein.
2 letal regulator proteins SrGAP3 (or WRP) and actin capping protein.
3 ssion of adducin3 (add3), which encodes an F-actin capping protein.
4 ed phosphorylation (Ser724) of adducin, an F-actin capping protein.
5 ssays, consistent with a role for Eps8 as an actin-capping protein.
6 of increased contractility following loss of actin-capping protein.
7 ces an actin phenotype similar to that of an actin-capping protein.
8 ctin binding and assembly while antagonizing actin-capping proteins.
9 n-related genes, such as GmACTIN, GmTUBULIN, actin capping protein 1 (GmCP1) and microtubule-associat
10 lament geometry, antagonizing the effects of actin-capping protein [5].
11 hibits the actin regulator Ena to activate F-actin Capping protein activity on inner membranes and th
12                         Manipulations of the actin-capping protein adducin in Drosophila and mammalia
13 ified the same self-peptides, derived from F-actin capping protein and beta-catenin.
14 In dynactin, the Arp1 filament is bounded by actin-capping protein at one end and a heterotetrameric
15 ocalized on endosomes together with the beta-actin capping protein, betacap73.
16       Here, we report an in vivo role of the actin-capping protein CAP-1 in the Caenorhabditis elegan
17 nts of the actin cytoskeleton, including the actin-capping proteins capping protein alpha and capping
18 d to a 12-residue peptide, TRTK-12, from the actin capping protein CapZ (alpha1 or alpha2 subunit, re
19 ization and depolymerization, resembling the actin capping protein CapZ.
20                              The filamentous actin-capping protein CapZ also associated with the SH3B
21 12-residue peptide (TRTK12) derived from the actin-capping protein CapZ.
22 0A1 and a peptide (TRTK-12) derived from the actin-capping protein CapZ.
23                                              Actin capping protein (CapZ) binds the barbed ends of ac
24 ointed end of the Arp1 minifilament, whereas actin capping protein (CapZ) is present at the barbed en
25  structural stability of F-actin through the actin capping protein, CapZbeta1, by promoting associati
26                                  Adducin, an actin-capping protein, colocalized with the actin rings.
27             CAPZA2 encodes a subunit of an F-actin-capping protein complex (CapZ).
28 characterizing the interaction of CD2AP with actin-capping protein CP.
29                                              Actin capping protein (CP) binds barbed ends of actin fi
30                                              Actin capping protein (CP) can be regulated by steric an
31 nd the alpha- and beta-heterodimers of the F-actin capping protein (CP) complex.
32 ichiometry and other structural information, actin capping protein (CP) is not present at the distal
33                        Cellular functions of actin capping protein (CP) regulators are poorly underst
34 P functions to facilitate the recruitment of actin capping protein (CP) to the Src kinase substrate,
35                         Here, we report that actin capping protein (CP), a regulator of actin filamen
36     CARMIL2 localizes to vimentin, regulates actin capping protein (CP), and binds to membranes.
37 ogic functions and structural correlates for actin capping protein (CP), we analyzed site-directed mu
38 lator in branched actin network formation is actin capping protein (CP), which binds to the barbed en
39 tures, which in turn efficiently release the actin-capping protein (CP) gelsolin from barbed actin en
40                            The heterodimeric actin-capping protein (CP) regulates actin assembly and
41                  CPI motifs bind directly to actin-capping protein (CP), and this interaction weakens
42 entire Arp filament core, which includes the actin capping protein, CP, to be determined for the firs
43 ilament nucleation in vitro In contrast, the actin capping protein Flightless-I, in conjunction with
44                  We examined the role of the actin-capping protein flightless I (FliI) in collagen re
45                   Tropomodulin (TMOD) is the actin-capping protein for the slow-growing end of filame
46 In the MPS, short actin filaments, capped by actin-capping proteins, form ring-like structures that w
47 ockdown of other actin regulators, including actin-capping protein genes and prefoldin subunit genes,
48  alters the subcellular distribution of an F-actin capping protein in the testis, supporting a role f
49  Thus, we uncovered a physiological role for actin-capping protein in regulating actomyosin contracti
50 izations of spectrin, actin, and adducin, an actin-capping protein, in the dendrites and soma of cult
51 iological regulators of mDia1, we found that actin-capping protein induced stable MTs in an mDia1-dep
52 tween the binding sites for three ligands: F-actin, Capping-Protein-Interacting (CPI) motifs, and V-1
53                      These results show that actin-capping protein is a novel regulator of MT stabili
54                        In contrast, Eps8, an actin capping protein, is seen most strongly at filopodi
55                 Here we report that Eps8, an actin-capping protein, is required for spine morphogenes
56 ous studies have identified mutations in the actin-capping protein KANK1 and the adaptor protein-4 co
57 ctly with and facilitates the recruitment of actin-capping protein, revealing barbed-end filament cap
58  CapZ ("capping protein") is a heterodimeric actin capping protein that blocks actin filament assembl
59                    Tropomodulin (Tmod) is an actin-capping protein that binds to the two tropomyosins
60                                  CAPZB is an actin-capping protein that caps the growing end of F-act
61    Tropomodulin-1 (Tmod-1) is a well defined actin-capping protein that interacts with tropomyosin (T
62        Tropomodulin (Tmod) is a cytoskeletal actin-capping protein that interacts with tropomyosin at
63                  Tropomodulin1 (Tmod1) is an actin-capping protein that plays an important role in ac
64            Adducin functions as a barbed-end actin capping protein to regulate actin filament length
65                The accumulation of actin and actin capping protein, which marks the site involved in
66 atially defined acetylation of heterodimeric actin capping protein, which we identify as an essential
67 locus that encodes the beta-subunit of the F-actin capping protein, while scorched mutations disrupt