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1 B virus ICP47 lacks a transporter-associated protein binding domain.
2 in has recently been implicated as a phospho-protein binding domain.
3 ructural changes primarily in the peripheral protein binding domain.
4 istent with its localization in a putative G-protein binding domain.
5 DNA-binding domain and a less well-conserved protein-binding domain.
6 assays showed that the LW motif is part of a protein-binding domain.
7 elix DNA-binding domain and a less conserved protein-binding domain.
8 acterized FHA domain appears to be a modular protein-binding domain.
9 e peptide structurally mimics a receptor's G protein-binding domain.
10 exible secondary structure, reminiscent of a protein-binding domain.
11 action is dependent on the presence of the G protein-binding domain.
12 oteins do not contain known globular protein-protein binding domains.
13 erturbation is transferred to the putative G protein binding domains.
14 e cluster but before the three major protein-protein binding domains.
15 gh their stomatin-like regions, which act as protein binding domains.
16 ems of the cation-pi complexes found at some protein binding domains.
17 ns involved in each process through distinct protein binding domains.
18 rotein, RB, contains at least three distinct protein binding domains.
19 ed for coding variants altering postsynaptic protein-binding domains.
20 dylinositol 3-phosphate- and arabinogalactan protein-binding domains.
21 odules, two of which correspond to predicted protein-binding domains.
22 of the plasma membrane by utilizing multiple protein-binding domains.
23  a 748-amino acid protein with two potential protein-binding domains.
24 with the presence or absence of specific Nck protein-binding domains.
25 well characterized phosphorylation-dependent protein-binding domains (14-3-3 and Src homology 2) and
26 This E7 activity depends on an intact pocket protein binding domain and a casein kinase II (CKII) pho
27 bitory domain that overlaps with its small G protein binding domain and that two separate activating
28 eal the structure of this versatile class of protein binding domains and provide a means for identify
29 he FRUA and FRUB proteins have a BTB protein-protein-binding domain and two zinc finger-like domains
30 main, two putative C-terminal retinoblastoma protein binding domains, and a nuclear hormone receptor
31 s, the C-terminal transactivation and pocket protein binding domains, and the internal marked box dom
32 nization of the dimers, in which the two pre-protein binding domains are located proximal to each oth
33                                    Such mini-protein binding domains are more amenable to synthetic c
34 nd its C-terminal oligomerization and capsid protein-binding domains are identical to those of UL26.5
35 the presence of numerous nucleic acid and/or protein binding domains, as do the two RNA ligases and a
36  involve the movement of flanking peripheral protein binding domains away from a shared dimerization
37    Immediately upstream of the promoter is a protein-binding domain between -146 and -121.
38  required the extracellular hemagglutinin (H-protein)-binding domain but not the cytoplasmic domain.
39 inding site spacing and orientation, and the protein-binding domain content that are important for th
40  determined to be a multifunctional DNA- and protein-binding domain (DPBD) that interacts with struct
41 -negative HeLa cells of ER alpha lacking the protein-binding domain for the AhR; and (c) mutation of
42 fied mwh as CG13913, which encodes a novel G protein binding domain-formin homology 3 (GBD-FH3) domai
43 GMP, evolved into the GK domain (GK(dom)), a protein-binding domain found in membrane associate guany
44 on that is bound by nucleolin as well as the protein binding domains important for bcl-2 mRNA recogni
45 e gene products is the presence of potential protein binding domains in the form of leucine-rich repe
46                                          The protein-binding domain in the BEL1 protein is located in
47 d involves an RNA domain highly similar to a protein-binding domain in the RNAs of RNase P/MRP.
48 tially unknown how the formation of sulfated protein-binding domains in HS can be regulated by microR
49 data imply that the BRCT domain is a phospho-protein binding domain involved in cell cycle control.
50 of functional and structural elements when a protein binding domain is evolved to a smaller functiona
51 usion protein composed of LUMP and a 5-kDa G protein binding domain is used as an FA sensor to quanti
52               The integrity of LXXLL and PDZ protein binding domains is important for activation of c
53  an increase in Cdk2 activity, if the pocket protein-binding domain is intact.
54 rides p21 in U2OS cells, provided the pocket protein-binding domain is intact; thus, this novel funct
55 n encodes six PDZ domains, which are protein-protein binding domains likely involved in protein clust
56 andidate oncogene with homology to a protein-protein binding domain of cyclin H.
57 rted that the noncatalytic carboxyl-terminal protein binding domain of focal adhesion kinase (FAK) is
58 ) modestly inhibited interaction between the protein binding domains of HIF-1alpha and p300.
59               A screen for inhibitors of the protein binding domains of p300 (CH1) and HIF-1alpha (C-
60  Taken together, these results show that the protein binding domains of RB are each regulated by dist
61 terminal CREB (cAMP response element-binding protein)-binding domain of the CREB regulator MECT1 (Muc
62 rone activity in vivo and that the essential protein-binding domain of GRP94 is distinct from the N-t
63               NMR studies show that the coat protein-binding domain of P22 scaffolding protein exhibi
64                                     The coat protein-binding domain of scaffolding protein is a helix
65                                   While many protein-binding domains of Axin have been identified, th
66 s independent of the Cdk- and retinoblastoma protein-binding domains of cyclin D1.
67 HLJ1 protein directly bound to catalytic and protein-binding domains of Src through its amino acid Y1
68  Dominant negative constructs containing the protein-binding domains of StBEL5 or POTH1 blocked the r
69 e gating steps in establishing growth factor protein-binding domains of these glycosaminoglycans.
70   Through deletion analysis, we identified a protein-binding domain present in the carboxy end of the
71 ed on the wild-type lambda, P22, and phi21 N protein binding domains ranging from 11 to 22 residues a
72 the RGS domain that contains an additional G protein-binding domain (RBD/GL).
73                                  Through its protein-binding domains, SLP-76 serves as a platform for
74                                      Protein-protein binding domains, such as Src homology 3 (SH3) do
75 se proteins typically contain DNA-binding or protein-binding domains, superstructure-forming repeats,
76 ifying RNA mutations in the 3'-terminal coat protein binding domain that increased or decreased RNA r
77                              SH3 domains are protein binding domains that occur widely among signal t
78                                     L27 is a protein-binding domain that can assemble essential prote
79  fragment thereof was conjugated to a target protein-binding domain that was capable of binding to a
80  guanylate kinases (MAGUKs) contain multiple protein-binding domains that allow them to assemble spec
81              Scaffold proteins often contain protein-binding domains that are connected in series by
82 roteins are characterized by a core motif of protein-binding domains that include a PDZ domain, a Src
83 id, spacer peptide 2, and p6 (which contains protein-binding domains that interact with host proteins
84 rase domain was inactivated or the Zn finger-protein binding domain was excised.
85 F1 protein-transactivating domain and the E2 protein-binding domain was able to reactivate lytic repl
86                                 The HCV core protein-binding domain was located within amino acid res
87 ssays, a PC1 C-terminal mutant lacking the G protein-binding domain was uncoupled from PC1-inhibited
88                 Vav proteins contain several protein binding domains which can link cell surface rece
89 nd functionally intact 14-3-3epsilon (YWHAE) protein-binding domain, which is directed to the nucleus
90 ch subunit also includes a larger peripheral protein binding domain with an alpha(+) beta-fold.
91 alization signal, and an eps15 homology (EH) protein-binding domain with an EF-hand motif at the C-te
92 ar factors, which is facilitated by multiple protein binding domains within pRb.
93 peptide is based on the native sequence of a protein-binding domain within a heteromeric transcriptio

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