ライフサイエンスコーパス: argininamide

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1 en bond donors from the guanidinium group of argininamide.

2 The ligands are argininamide, a linear peptide mimic of the Tat basic do

3 as compared to single-charge lysinamide and argininamide adsorbents of matched total charge.

4 ed in and around the known binding sites for argininamide and a BIV Tat arginine-rich peptide, respec

5 was remarkably similar to that obtained for argininamide and is evidence for guanidinoneomycin bindi

6 Argininamide and its analogs are known to bind to the ha

7 o-axially stack and the critical U23 and the argininamide are located in the major groove.

8 ncy virus type-1 (HIV-1) bound to the ligand argininamide (ARG) has been characterized using a combin

9 s) both in free form and bound to the ligand argininamide (ARG).

10 xo -1,2-diphenyl-3H-1,2,4-triazol-4-yl]ethyl]argininamide (BIIE0246) not only blocked the effects of

11 Argininamide binding is stabilized by stacking of the gu

12 hat the base triple is required for specific argininamide binding.

13 ple mutant of the three base bulge HIV-1 TAR-argininamide complex demonstrated that the base triple i

14 The dynamics of the HIV-2 TAR-argininamide complex was investigated by measurements of

15 e high resolution structure of the HIV-2 TAR-argininamide complex, confirming that a base triple is a

16 frequencies of base motion in the HIV-2 TAR-argininamide complex.

17 n the HIV-2 transactivation response element-argininamide complex.

18 gh resolution NMR structure of the HIV-2 TAR-argininamide complex.

19 ved than in earlier studies of the HIV-1 TAR-argininamide complex.

20 mine the solution structure of the HIV-2 TAR-argininamide complex.

21 The argininamide guanidium group hydrogen bonds to the major

22 Binding of argininamide induces formation of one Watson-Crick and t

23 The studies reveal that the argininamide inhibitory mechanism involves a shift of th

24 e data suggest a molecular mechanism wherein argininamide inhibits NC-facilitated TAR RNA/DNA anneali

25 se triple is an important feature of the TAR-argininamide interaction.

26 Here, we explore how argininamide modulates the annealing kinetics and second

27 d to examine how a model inhibitor of HIV-1, argininamide, modulates the nucleic acid chaperone activ

28 result contradicts the belief that a single argininamide residue is responsible for stabilising the

29 between the bases of A22 and U23, forming an argininamide sandwich.

30 The complex of TAR with argininamide serves as a model for the RNA conformation

31 Analogues of the argininamide-type NPY Y1 receptor (Y1R) antagonist BIBP3

32 ergoes the largest dynamic change on binding argininamide, while U25 remains flexible, reflecting the

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