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1 e LKB1 polyubiquitination by activating Skp2-SCF ubiquitin ligase.
2  remove Nedd8 from Cullin1, a subunit of the SCF ubiquitin ligase.
3 n regulating the activity of Cul1-containing SCF ubiquitin ligases.
4 mechanism underlying E2 selection by VHL and SCF ubiquitin ligases.
5 d Skp1 proteins in reconstitution of VHL and SCF ubiquitin ligases.
6 otheses for how CSN promotes the activity of SCF ubiquitin ligases.
7  tobacco extracts was shown to interact with SCF ubiquitin ligases.
8 -like protein Nedd8 from the Cul1 subunit of SCF ubiquitin ligases.
9 (deneddylation) from the cullin component of SCF ubiquitin ligases.
10 recognition by the Skp1-Cdc53-F-box protein (SCF) ubiquitin ligase.
11  hydroxylate Pro143 of Skp1, a subunit of E3(SCF)ubiquitin-ligases.
12 sylation of DdSkp1, an adaptor subunit in E3(SCF) ubiquitin ligases.
13 te recognition subunit of SKP1-CULLIN-F-box (SCF) ubiquitin ligases.
14  other core components of Skp1-Cullin-F-box (SCF) ubiquitin ligases.
15                We conclude that CSN inhibits SCF ubiquitin ligase activity in targeting p27 proteolys
16  into the role of CAND1 in the regulation of SCF ubiquitin-ligase activity.
17 hese data indicate that Skp1 and possibly E3(SCF)ubiquitin-ligase activity modulate O(2)-dependent cu
18 , CAND1 regulated the assembly of productive SCF ubiquitin ligases, allowing a common CUL1-ROC core t
19 W7 is the substrate-recruiting subunit of an SCF ubiquitin ligase and a major tumor-suppressor protei
20                            It interacts with SCF ubiquitin ligases and deconjugates Nedd8/Rub1 from c
21 dditional layer for substrate recruitment by SCF ubiquitin ligases and provide conceptual insight int
22        Skp1 is an adaptor-like protein in E3(SCF)-ubiquitin ligases and other multiprotein complexes
23 Archipelago (Ago), the F box component of an SCF-ubiquitin ligase and the Drosophila ortholog of a hu
24 ly binds Skp1 protein (a 'core' component of SCF ubiquitin ligase), and phosphorylated IkappaB(alpha)
25                                              SCF ubiquitin ligases are composed of a core of conserve
26 (s) as the target of the SKP1-Cullin1-F Box (SCF) ubiquitin ligases assembled with AUF1/2.
27 auxin regulates gene expression by promoting SCF ubiquitin-ligase-catalysed degradation of the Aux/IA
28                                          The SCF ubiquitin ligases catalyze protein ubiquitination in
29 a suggest that hCUL1 functions as part of an SCF ubiquitin ligase complex in human cells.
30 es encode several components involved in the SCF ubiquitin ligase complex including a viral Skp1 homo
31                                          The SCF ubiquitin ligase complex of budding yeast triggers D
32                                          The SCF ubiquitin ligase complex regulates diverse cellular
33 1 interacts with beta-TrCP, a subunit of the SCF ubiquitin ligase complex that mediates the degradati
34 directly with the Skp1 component of the host SCF ubiquitin ligase complex, and that the binding of M-
35 epeat-containing protein, a component of the SCF ubiquitin ligase complex, previously shown to be req
36 ning protein (beta-TrCP), a component of the SCF ubiquitin ligase complex, to p100.
37 expression of Skp2 and Cks1, subunits of the SCF ubiquitin ligase complex, which ubiquitinates p27(Ki
38 argets YAP1 for degradation via the betaTrCP-SCF ubiquitin ligase complex.
39 erved F box protein, suggesting a role in an SCF ubiquitin ligase complex.
40  and consequent loss of its affinity for the SCF ubiquitin ligase complex.
41 x proteins act as bridging components of the SCF ubiquitin ligase complex; the N-terminal F-box binds
42                                          The SCF ubiquitin-ligase complex targets the ubiquitin-media
43 Gli2 interacts directly with betaTrCP in the SCF ubiquitin-ligase complex through two binding sites,
44 city factor for the Skp1-Cul1-F-box protein (SCF) ubiquitin ligase complex and targets several protei
45 al degradation by a SKP1-CUL1-F-box protein (SCF) ubiquitin ligase complex that contains the orphan F
46 cificity for the Skp1-Cullin1-F-box protein (SCF) ubiquitin ligase complex that targets multiple onco
47 ificity subunits of the Skp1-Cullin 1-F-box (SCF) ubiquitin ligase complex that targets these CDKI pr
48 group are members of the Skp, Cullin, F box (SCF) ubiquitin ligase complex.
49 s analogous to the cellular Skp1-Cul1-F-box (SCF) ubiquitin ligase complex.
50  component of the Skp1-Cullin-F-box protein (SCF) ubiquitin-ligase complex (SCF(skp2)).
51 hosphorylation of Ci/Gli triggers binding to SCF ubiquitin ligase complexes and consequent proteolysi
52 equired Skp2, a substrate-binding subunit of SCF ubiquitin ligase complexes, but also relied on CHIP,
53 rone system to the substrate-specific arm of SCF ubiquitin ligase complexes, suggesting a role in SCF
54 nt development by modulating the activity of SCF ubiquitin ligase complexes.
55  and for defining new modes of regulation of SCF ubiquitin ligase complexes.
56 -like molecule is control of the activity of SCF ubiquitin ligase complexes.
57 TRCP, all of which function as components of SCF ubiquitin-ligase complexes.
58 function in Skp1-Cdc53/Cullin-F-box protein (SCF) ubiquitin ligase complexes.
59                                              SCF ubiquitin ligases, composed of three major subunits,
60                                              SCF ubiquitin ligases contain an E3 core composed of Skp
61                                              SCF ubiquitin ligases control various processes by marki
62                     Skp1-Cul1-F-box protein (SCF) ubiquitin ligases direct cell survival decisions by
63  F box protein Nutcracker, a component of an SCF ubiquitin ligase (E3) required for caspase activatio
64                                           In SCF ubiquitin ligases, F-box proteins serve as substrate
65  Release of ubiquitin-charged Cdc34 from the SCF ubiquitin ligase followed by diffusion-driven collis
66 ction of CSN is to maintain the stability of SCF ubiquitin ligases in vivo.
67 een for substrates of the Skp1-cullin-F-box (SCF) ubiquitin ligase in mammalian cells.
68 t K63-linked LKB1 polyubiquitination by Skp2-SCF ubiquitin ligase is critical for LKB1 activation by
69 rovide evidence that E2 selection by VHL and SCF ubiquitin ligases is determined not solely by the Cu
70  proteins in E3 Skp1/Cullin-1/F-box protein (SCF) ubiquitin ligases is well characterized.
71 te recognition component of Skp1-Cul1-F-box (SCF) ubiquitin ligase, played an essential and specific
72 rate binding subunit of a Skp1/Cullin/F Box (SCF) ubiquitin ligase, regulates the abundance of the gl
73 tes in order to allow its recognition by the SCF ubiquitin ligase subunit Cdc4.
74 ation and subsequent glycosylation of the E3(SCF) ubiquitin ligase subunit Skp1 affects its conformat
75 ied Sic1, a prototype substrate of the Cdc34/SCF ubiquitin ligase, suggests that substrate degradatio
76 bw7 is the substrate-binding component of an SCF ubiquitin ligase that degrades critical oncoproteins
77 codes the substrate recognition subunit of a SCF ubiquitin ligase that targets proteins for degradati
78 -specific substrate recognition component of SCF ubiquitin ligases that catalyzes the ubiquitination
79 is an F-box constituent of Skp-Cullin-F-box (SCF) ubiquitin ligases that directs ubiquitylation of cy
80 is a component of Skp1-Cullin-F-box protein (SCF) ubiquitin ligases that target regulatory proteins f
81  Ams2 destruction via both the APC/C and the SCF ubiquitin ligases underlies the coordination of hist
82 yclin D1 is recognized by a Skp1-Cul1-F box (SCF) ubiquitin ligase where FBX4 and alphaB crystallin g
83                         Remarkably, the Skp2-SCF ubiquitin ligase, which plays a central role in cell
84 LORAL ORGANS (UFO), an F-box component of an SCF ubiquitin ligase, yet how this regulation is effecte

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