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1 phenylamidines were investigated along with netropsin.
2 be blocked by the minor groove binding drug netropsin.
3 pin of sequence 5'-CGAATTCGTCTCCGAATTCG) and netropsin.
4 duplex DNA are unaffected by the addition of netropsin.
5 ercoiled form by ligation in the presence of netropsin.
6 DNA upon binding of the minor groove binder netropsin.
7 d cytotoxicity can be inhibited in vivo with netropsin, a potent competitive inhibitor of binding of
9 ferential duplex affinity exhibited by 5PTB, netropsin and 4',6-diamidino-2-phenylindole (DAPI), two
10 between two minor groove binding compounds, netropsin and 4,6-diamidino-2-phenylindole (DAPI), and a
11 binding ligands (Hoechst 33258, distamycin, netropsin and berenil) with DNA fragments which have bee
14 ructures of the two duplexes, in contrast to netropsin and DAPI, which bind with similar affinities t
15 a series of bis-linked lexitropsins based on netropsin and distamycin have been screened for their ef
18 data have shown cooperativity of binding for netropsin and Hoechst 33258 and have provided ligand:DNA
19 eir association to the (AATT)2 binding site, netropsin and pentamidine acquire 26+/-3 and 34+/-2 addi
20 gineered a crystal designed to position both netropsin and the polyamide at two distinct locations wi
21 ss of compounds is related to the linked bis-netropsins and bis-distamycins, but here, only one amino
22 y, a representative DNA minor-groove binder (netropsin) and ligands binding DNA base-pairing defects
23 d that minor groove-binding ligands berenil, netropsin, and distamycin and the intercalating ligand a
24 groove binding ligands, such as distamycin, netropsin, and GLX, an indole-linked dimer of netropsin,
26 GCAAATTTGCGC)2 also forms two complexes with netropsin, and the complex with weaker affinity is again
29 ook 2 (HMGA2) as the protein of interest and netropsin as the inhibitor of HMGA2-DNA interactions.
30 immobilize the molecules DAPI, Hoechst, and netropsin at defined positions in the lattice, allowing
31 eveloped: (i) two different bound species of netropsin at single binding sites and (ii) a netropsin i
41 elty of the structures is that there are two netropsins bound end-to-end in the minor groove of each
42 S) with nanoscale ion emitters indicate that netropsin can simultaneously and sequentially bind to bo
43 etropsin, and GLX, an indole-linked dimer of netropsin, can effectively disrupt the UL9-DNA complex o
45 The asymmetric unit of the RT fragment-DNA-netropsin crystals contains one protein molecule and one
46 y for several agents including distamycin A, netropsin, DAPI, Hoechst 33258, and berenil is described
48 tries, AT sequence specific ligands, such as netropsin, distamycin, and GLX, prefer uniform, narrow m
49 We compare this structure to other Class I netropsin-DNA structures and find that the asymmetry of
52 es were in excellent agreement; for example, netropsin/DNA formation constants were determined to be
57 of the DNAs investigated clearly shows that netropsin forms two different complexes at AATT sites, a
59 ts with minor groove binding agents, such as netropsin, have provided detailed, atomic level views of
60 andactinomycin D) and minor groove binders (netropsin, Hoechst 33258 and distamycin) has shown the s
63 halpy and heat capacity changes suggest that netropsin interacts similarly with these two oligonucleo
68 inding reactions involving the ligands DAPI, netropsin, lexitropsin, and the lambda repressor binding
73 By contrast, the binding to either duplex of netropsin or DAPI induces little or no change in the ele
75 groove binding agents (DAPI, distamycin, and netropsin) showed a strong preference for AT-rich duplex
76 ded by this screening excise, we showed that netropsin, the specific inhibitor of HMGA2-DNA interacti
77 dynamically distinct complexes on binding of netropsin to a number of hairpin-forming DNA sequences c
79 ng interactions from the amide groups of the netropsin to the A x T base pairs of the minor groove.
80 However, and relative to ATT, binding of netropsin to the hydrophobic groove has a decreased bind
86 nucleotide contains two AATT sites that bind netropsin with flanking 5' and 3' sequences that are not
89 lutes and DNA sequence on the interaction of netropsin with three duplexes has been studied by isothe
90 AATT site contributes to the orientation of netropsin within the groove while hydrogen bonding patte