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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 n cross sections in agreement with a general beta-barrel structure.
7 ly of a helix lying outside of the lipocalin beta-barrel structure.
8 of ions, and are characterized by a trimeric beta-barrel structure.
9 ong excitonic coupling, is limited by the FP beta-barrel structure.
10 ce that forms a tightly folded anti-parallel beta-barrel structure.
11  a proposal that the capsid protein adopts a beta-barrel structure.
12 evalent in the "aromatic bands" of the porin beta barrel structures.
13 a structure; while domain 2 and domain 3 are beta-barrel structures.
14  The outer membrane contains proteins with a beta-barrel structure(1,2).
15 ne-spanning segment that folds into a unique beta barrel structure and inserts into the membrane by a
16 ues are secreted factors that share a common beta-barrel structure and act on target cells by binding
17             TrmO has a unique single-sheeted beta-barrel structure and does not belong to any known c
18 ding may be accompanied by opening of the P2 beta-barrel structure and ligand exchange with the appos
19 serts into the bacterial outer membrane as a beta-barrel structure and mediates secretion of the pass
20 in which the subunits have a classical alpha/beta-barrel structure and Mr 39,212 Da.
21 arger oligomers of these fragments may adopt beta-barrel structures and that beta-barrels can be form
22 ite and a partial flexibility of the protein beta-barrel structure) and provide the first evidence th
23  missing one of the 11 beta-strands from its beta-barrel structure, and in two of the variants, addin
24     Integral transmembrane proteins assume a beta-barrel structure, and their assembly is catalyzed b
25  more exposed positions at the apexes of the beta-barrel structure are most in-line with the experime
26             CspA consists of a five-stranded beta-barrel structure containing two RNA-binding motifs,
27                               The pr peptide beta-barrel structure covers the fusion loop in E, preve
28                       Larger than any of the beta-barrel structures determined to date by magic-angle
29 s of pH showed that amide protons within the beta-barrel structure exchange at the EX2 limit, consequ
30 nus of helix alpha1 and perturbations in the beta-barrel structure, exhibits fraying of three residue
31                Our results indicate that the beta-barrel structure extends beyond the bilayer and inv
32      The West Nile domain III structure is a beta-barrel structure formed from seven anti-parallel be
33      The dimeric interface is dominated by a beta-barrel structure, formed by face-to-face packing of
34 guided by similar global parameterization of beta barrel structures has been less successful, likely
35 ormational changes to generate a heptameric, beta-barrel structure in host membranes.
36         The similarity between M156R and the beta-barrel structure in the N terminus of eIF2alpha sug
37 ut not exclusively, in what are likely to be beta-barrel structures in the capsid protein VP3.
38 he NMR structure of sortase reveals a unique beta-barrel structure, in which the active-site sulfhydr
39 ot cleaved to form VP2 and VP4, so the 'VP2' beta-barrel structure is complemented with a unique exte
40 affolds have been shown to mimic the protein beta-barrel structure, maintaining green fluorescence re
41 nd pore-forming toxins, because their robust beta-barrel structure makes them the best choice for dev
42 n and deletion mutational analyses support a beta-barrel structure model with an N-terminal globular
43 erminal arm folds back onto itself to form a beta-barrel structure nearly identical to its dimeric co
44 eria and Archaea, do not exhibit the typical beta-barrel structure of Cyc2.
45 s to a region located in the open end of the beta-barrel structure of IL-1beta and blocks binding of
46                     The predicted C-terminal beta-barrel structure of TGD4 is weakly similar to prote
47  ligand were located at the entrance of each beta-barrel structure of the dimer.
48 h a glutamine-rich motif on the conserved VP beta-barrel structure of variants incompatible with AAP2
49 utperforms all other methods for accuracy of beta-barrel structure prediction.
50 l portion of delta, which forms a jelly-roll beta barrel structure, regulates membrane penetration by
51 (SH3) domain in class II myosins, a distinct beta-barrel structure, remains unknown.
52 ins 1-3 and 11 are known to have a conserved beta-barrel structure similar to that of avidin and the
53 sphorylase (PNPase), which also folds into a beta-barrel structure similar to that of CspA.
54 FABPc of schistosomes is predicted to form a beta-barrel structure similar to the mammalian family of
55 as typical porins are trimers with extensive beta-barrel structure, size exclusion chromatography and
56                Alt a 1 has a unique, dimeric beta-barrel structure that appears to define a new prote
57 mental decoherence because of the protective beta-barrel structure that encapsulates the fluorophore
58  domain), which has been predicted to have a beta-barrel structure that interacts with and stabilizes
59 a-sandwiches fold, with a core, six-stranded beta-barrel structure that is also found in the hepatiti
60  show that AvrE-family effectors fold into a beta-barrel structure that resembles bacterial porins.
61  and MNV, three loops connecting the central beta-barrel structure were found to be responsible for t
62 dy showed that NspA adopts an eight-stranded beta-barrel structure when reconstituted in detergent.
63 Common to autofluorescent FPs is their tight beta-barrel structure, which provides the rigidity and c
64 sidues primarily located in both lids of the beta-barrel structure, which suggests that small scale s
65   MTCP-1 folds into a compact eight-stranded beta barrel structure with a short helix between the fou
66 e revealed that V1V2 assumes a five-stranded beta barrel structure with the region of the integrin-bi
67  Urinary Proteins (MUPs) contain a conserved beta-barrel structure with a characteristic central hydr
68 al analysis indicated that Der p 13 adopts a beta-barrel structure with a predominately apolar pocket
69                                   It forms a beta-barrel structure with five anti-parallel beta-stran
70 s demonstrated that the TpsB protein forms a beta-barrel structure with pore forming activity and fac
71 om Aquifex aeolicus revealed an antiparallel beta-barrel structure, with three helices packed outside