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1 eby forming a direct precursor for the alpha/beta barrel structure.
2 nt domain at the C terminus with a predicted beta-barrel structure.
3 ty of the two proteins was consistent with a beta-barrel structure.
4 bic pocket that is located at the end of its beta-barrel structure.
5 c motif that is positioned at the end of the beta-barrel structure.
6 ly of a helix lying outside of the lipocalin beta-barrel structure.
7 of ions, and are characterized by a trimeric beta-barrel structure.
8 ce that forms a tightly folded anti-parallel beta-barrel structure.
9  a proposal that the capsid protein adopts a beta-barrel structure.
10 evalent in the "aromatic bands" of the porin beta barrel structures.
11 a structure; while domain 2 and domain 3 are beta-barrel structures.
12 ues are secreted factors that share a common beta-barrel structure and act on target cells by binding
13             TrmO has a unique single-sheeted beta-barrel structure and does not belong to any known c
14 serts into the bacterial outer membrane as a beta-barrel structure and mediates secretion of the pass
15 in which the subunits have a classical alpha/beta-barrel structure and Mr 39,212 Da.
16 arger oligomers of these fragments may adopt beta-barrel structures and that beta-barrels can be form
17 ite and a partial flexibility of the protein beta-barrel structure) and provide the first evidence th
18  missing one of the 11 beta-strands from its beta-barrel structure, and in two of the variants, addin
19     Integral transmembrane proteins assume a beta-barrel structure, and their assembly is catalyzed b
20  more exposed positions at the apexes of the beta-barrel structure are most in-line with the experime
21             CspA consists of a five-stranded beta-barrel structure containing two RNA-binding motifs,
22                               The pr peptide beta-barrel structure covers the fusion loop in E, preve
23 s of pH showed that amide protons within the beta-barrel structure exchange at the EX2 limit, consequ
24 nus of helix alpha1 and perturbations in the beta-barrel structure, exhibits fraying of three residue
25                Our results indicate that the beta-barrel structure extends beyond the bilayer and inv
26      The West Nile domain III structure is a beta-barrel structure formed from seven anti-parallel be
27      The dimeric interface is dominated by a beta-barrel structure, formed by face-to-face packing of
28 ormational changes to generate a heptameric, beta-barrel structure in host membranes.
29         The similarity between M156R and the beta-barrel structure in the N terminus of eIF2alpha sug
30 ut not exclusively, in what are likely to be beta-barrel structures in the capsid protein VP3.
31 he NMR structure of sortase reveals a unique beta-barrel structure, in which the active-site sulfhydr
32 ot cleaved to form VP2 and VP4, so the 'VP2' beta-barrel structure is complemented with a unique exte
33 affolds have been shown to mimic the protein beta-barrel structure, maintaining green fluorescence re
34 nd pore-forming toxins, because their robust beta-barrel structure makes them the best choice for dev
35 n and deletion mutational analyses support a beta-barrel structure model with an N-terminal globular
36 erminal arm folds back onto itself to form a beta-barrel structure nearly identical to its dimeric co
37 s to a region located in the open end of the beta-barrel structure of IL-1beta and blocks binding of
38                     The predicted C-terminal beta-barrel structure of TGD4 is weakly similar to prote
39 utperforms all other methods for accuracy of beta-barrel structure prediction.
40 l portion of delta, which forms a jelly-roll beta barrel structure, regulates membrane penetration by
41 (SH3) domain in class II myosins, a distinct beta-barrel structure, remains unknown.
42 ins 1-3 and 11 are known to have a conserved beta-barrel structure similar to that of avidin and the
43 sphorylase (PNPase), which also folds into a beta-barrel structure similar to that of CspA.
44 FABPc of schistosomes is predicted to form a beta-barrel structure similar to the mammalian family of
45 as typical porins are trimers with extensive beta-barrel structure, size exclusion chromatography and
46                Alt a 1 has a unique, dimeric beta-barrel structure that appears to define a new prote
47 mental decoherence because of the protective beta-barrel structure that encapsulates the fluorophore
48  domain), which has been predicted to have a beta-barrel structure that interacts with and stabilizes
49 a-sandwiches fold, with a core, six-stranded beta-barrel structure that is also found in the hepatiti
50  and MNV, three loops connecting the central beta-barrel structure were found to be responsible for t
51 dy showed that NspA adopts an eight-stranded beta-barrel structure when reconstituted in detergent.
52 Common to autofluorescent FPs is their tight beta-barrel structure, which provides the rigidity and c
53 sidues primarily located in both lids of the beta-barrel structure, which suggests that small scale s
54   MTCP-1 folds into a compact eight-stranded beta barrel structure with a short helix between the fou
55 e revealed that V1V2 assumes a five-stranded beta barrel structure with the region of the integrin-bi
56 al analysis indicated that Der p 13 adopts a beta-barrel structure with a predominately apolar pocket
57                                   It forms a beta-barrel structure with five anti-parallel beta-stran
58 s demonstrated that the TpsB protein forms a beta-barrel structure with pore forming activity and fac
59 om Aquifex aeolicus revealed an antiparallel beta-barrel structure, with three helices packed outside

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