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1 X-isoleucine-proline) which exists within an intrinsically disordered region.
2 erent interacting partners that bind through intrinsically disordered regions.
3 er DMS reactivity than regions that code for intrinsically disordered regions.
4 transmembrane domains (TMDs) with or without intrinsically disordered regions.
5 ch has general applicability to the study of intrinsically disordered regions.
6 egions (PFRs), including protein domains and intrinsically disordered regions.
7 ar interactions in multidomain proteins with intrinsically disordered regions.
8 t are multivalent or contain low-complexity, intrinsically disordered regions.
9 Both contain three folded domains and ~70% intrinsically disordered regions.
10 w that 21.7% of them are located within such intrinsically disordered regions.
11 ic, multidomain proteins with structured and intrinsically disordered regions.
12 condary structure and natively unstructured (intrinsically disordered) regions.
15 yltransferase activity and is composed of an intrinsically disordered region and a folded segment.
16 s of VP30 with sequence features that typify intrinsically disordered regions and a putative RNA bind
17 y motor and structural proteins that contain intrinsically disordered regions and coiled coil domains
18 re of the Pih1 C terminus and identified two intrinsically disordered regions and five hydrophobic cl
19 ss than ten residues in length, occur within intrinsically disordered regions, and are recognized and
21 Nonoptimal codons are preferentially used in intrinsically disordered regions, and more optimal codon
22 ements in client proteins stabilizes Hsp33's intrinsically disordered regions, and this stabilization
26 bacterial ParB forms an elongated dimer with intrinsically disordered regions as well as folded domai
28 t a conserved Ser-46 site in the N-terminal "intrinsically disordered" region by IkappaB kinase epsil
29 d and cdk-dependent phosphorylation of these intrinsically disordered regions contributes to Ngn2 reg
30 the two domains, along with the presence of intrinsically disordered regions, controls this process.
31 hydrogen-bonded structure and may provide an intrinsically disordered region for chaperone interactio
32 idated the molecular principles by which its intrinsically disordered region (IDR) at the carboxyl-te
33 polypeptide's N-terminal end, composed of an intrinsically disordered region (IDR) followed by a high
34 actions between unphosphorylated PhyR and an intrinsically disordered region (IDR) of the anti-sigma
38 ted mutagenesis indicated that one predicted intrinsically disordered region IDR2 is involved in Tah1
39 at histone chaperones are highly enriched in intrinsically disordered regions (IDRs) and acidic stret
42 ins are composed of both modular domains and intrinsically disordered regions (IDRs) having low amino
44 iochemical evidence that SLC26 proteins have intrinsically disordered regions (IDRs) in their C-termi
46 re enriched in transcript sequences encoding intrinsically disordered regions (IDRs) of proteins, in
47 mains, about half of the protein consists of intrinsically disordered regions (IDRs) of varying lengt
50 able fraction of eukaryotic proteins contain intrinsically disordered regions (IDRs), which act in un
51 he identification of proteins with extensive intrinsically disordered regions (IDRs), which are confo
58 o inactive, liquid-like droplets through its intrinsically disordered regions in the N-terminal domai
59 rties to protein structural properties, i.e. intrinsically disordered regions in the protein chain.
61 K1 uses an N-terminal extension and a large, intrinsically disordered region juxtaposed to a stable s
63 ions that encode protein domain junctions or intrinsically disordered regions may reflect increased R
64 anisms may therefore help us to decipher how intrinsically disordered regions mediate functional effe
67 ined secondary structural elements and is an intrinsically disordered region of the channel protein.
69 supporting interesting parallels between the intrinsically disordered regions of histones and this po
70 ediated by NPCs are focused on properties of intrinsically disordered regions of nucleoporins that bi
73 Tmod1-TM complex formation, indicating that intrinsically disordered regions of the two proteins bec
75 tal approaches identified several conserved, intrinsically disordered regions outside the homeodomain
76 a bipartite nuclear localization signal, an intrinsically disordered region overlapping arginine-ric
78 cal doctrine, in which phosphorylation of an intrinsically disordered region/protein confers affinity
79 y between folded domains, linear motifs, and intrinsically disordered regions regulates the formation
80 secondary structure, transmembrane helices, intrinsically disordered regions, signal peptides and ot
82 tructural evidence that Ngn2 contains large, intrinsically disordered regions that undergo phosphoryl
83 xperiments show that despite being within an intrinsically disordered region, the hinge E7 epitope ha
84 ronmentally sensitive folding pathway and an intrinsically disordered region, the yeast prion protein
85 e mass spectrometry data, and on the role of intrinsically disordered regions to control protein moti
87 the protein's functional regions (domains or intrinsically disordered regions) to find those that sho
88 Nearly half of the RNA-binding sites map to intrinsically disordered regions, uncovering unstructure
89 determine whether these C-terminal tails are intrinsically disordered regions, we conducted a battery
92 ment structural transitions occurring within intrinsically disordered regions, with regions involved
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