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1 mCystin, that contains ankyrin repeats and a sterile alpha motif.
2 cortactin SH3 domain-binding peptides and a sterile alpha motif.
3 d in the p63 carboxyl-terminal region with a sterile alpha-motif.
4 ruitment, highlighting the essential role of Sterile Alpha Motifs.
5 ymerases, we have detected new HhH motifs in sterile alpha motif and barrier-to-autointegration facto
13 h results from the cellular dNTP hydrolyzing sterile alpha motif and histidine aspartic domain contai
16 e triphosphate triphosphohydrolase (dNTPase) sterile alpha motif and histidine/aspartic domain-contai
17 ctor in stressful conditions, the MAP3K ZAK (Sterile alpha motif and leucine zipper-containing kinase
19 Odin, contains several ankyrin repeats, two sterile alpha motifs and a phosphotyrosine binding domai
20 ), TRIF-related adapter molecule (TRAM), and sterile alpha motifs and beta-catenin/armadillo repeats
21 d identity with TANK1 in the ankyrin repeat, sterile alpha-motif, and PARP catalytic domains but has
22 ed tRNA-binding domain of Tric1 and Tric2, a sterile-alpha-motif at the C-terminal end of the protein
23 degeneration upon knockdown of Sarm1 [SARM (sterile alpha-motif-containing and armadillo-motif conta
24 ure of DprA consists of the association of a sterile alpha motif domain and a Rossmann fold and that
27 e, using proteomic strategies, we identified sterile alpha motif domain containing 9 (SAMD9), an inte
28 nse mutation (c.2640C>A, p.His880Gln) in the sterile alpha motif domain containing 9-like gene (SAMD9
31 is similar to the ssRNA-binding site of the sterile alpha motif domain of the Saccharomyces cerevisi
32 embrane domains, multiple ankyrin repeats, a sterile alpha motif domain, and a potential PDZ-binding
35 o identify de novo heterozygous mutations in sterile alpha motif domain-containing protein 9 (SAMD9,
37 associates constitutively via an N-terminal sterile-alpha motif domain with Ste11, and this interact
38 expression of the dominant-negative Scm-SAM (sterile alpha motif) domain both affected the binding pa
41 iddleman of seventy-eight signaling), a SAM (sterile alpha motif) domain-containing cofactor that req
42 anslocation, which fuses the N-terminal SAM (sterile alpha-motif) domain of the ETV6 (or TEL) transcr
43 Deletion of the C-terminal coiled-coil and sterile alpha motif domains abolished neurabin I dimeriz
44 nkyrin repeats, a single SH3 domain, and two sterile alpha motif domains followed by a long proline-r
47 with the p63alpha carboxyl terminus and its sterile alpha-motif, including the apobec-1-binding prot
48 , we have characterized a membrane-targeting sterile alpha motif-like domain in the amino terminus of
50 Domain deletion analysis showed that the sterile alpha-motif of Mst50 but not the Ras-association
51 dies previously revealed that the N-terminal sterile alpha motif (or SAM) domain of SMSr drives self-
52 In contrast, mutation of either the SAM (sterile alpha motif) or TIR (Toll-interleukin-1 receptor
53 n, which is structurally similar to the SAM (sterile alpha motif) protein-protein interaction domain,
54 s), Eph receptors are unique in possessing a sterile alpha motif (SAM domain) at their C-terminal end
55 atalytic domain flanked by an amino-terminal sterile alpha motif (SAM) and a carboxyl-terminal START
56 m has an extended C terminus consisting of a sterile alpha motif (SAM) and an extreme C terminus, it
59 also generated MST11 mutant alleles with the sterile alpha motif (SAM) and Ras-association (RA) domai
67 own that tankyrase 1 polymerizes through its sterile alpha motif (SAM) domain to assemble large prote
68 13, Tyr-128, and Tyr-145, "3Y") as well as a sterile alpha motif (SAM) domain whose function is uncle
69 give rise to amino acid substitutions in the sterile alpha motif (SAM) domain, and are predicted to a
70 teraction, which requires the Scm C-terminal sterile alpha motif (SAM) domain, is crucial for the eff
74 tructures of the polymerizing TNKS and TNKS2 sterile alpha motif (SAM) domains, revealing versatile h
76 isrupting the polymerization activity of the sterile alpha motif (SAM) of the PcG protein Polyhomeoti
77 mical studies have shown that the N-terminal sterile alpha motif (SAM) of Yan is able to self associa
78 olling Ph function through modulation of its sterile alpha motif (SAM) polymerization leading to the
79 N-terminal KH domains, whereas a C-terminal sterile alpha motif (SAM) self-polymerizes in vitro and
80 encoded by ubc2 shows localized homology to Sterile Alpha Motif (SAM), Ras Association (RA) and Src
81 cruited to activated EphA2 via a heterotypic sterile alpha motif (SAM)-SAM domain interaction, leadin
82 structure of SHD2 identifies the domain as a sterile alpha-motif (SAM) domain and shows a propensity
83 rm::Polo interaction in vivo, we show that a sterile alpha-motif (SAM) domain located at the C termin
85 ion of Dlx3 is abrogated by mutations in the sterile alpha-motif (SAM) domain of p63 that are associa
86 we identify and characterize the Drosophila sterile alpha-motif (SAM) domain-containing protein Cask
88 ure of n-NafY reveals that it belongs to the sterile alpha-motif (SAM) family of domains, which are f
89 TEL1, self-associates through an N-terminal sterile alpha-motif (SAM), leading to speculation that Y
91 tudies, several mutations in the cytoplasmic sterile-alpha-motif (SAM) domain of human EPHA2 on chrom
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