ライフサイエンスコーパス: alpha-neurotoxin

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1 gnate peptide and alpha-bungarotoxin, a long alpha-neurotoxin.

2 or interactions and the orientation of bound alpha-neurotoxin.

3 he binding and functional activity of a long alpha-neurotoxin.

4 which permitted the evolution of snake venom alpha-neurotoxins.

5 re with the biological action of short-chain alpha-neurotoxins.

6 sociation of agonists and slow rates for the alpha-neurotoxins.

7 forms a major determinant for the binding of alpha-neurotoxins.

8 inhibition mechanism by snake-venom-derived alpha-neurotoxins.

9 Arg36, a residue that is invariant among all alpha-neurotoxins.

10 ariant in kappa-neurotoxins and not found in alpha-neurotoxins.

11 neuronal membrane molecule related to snake alpha-neurotoxins able to modulate nAChRs.

12 ing for alpha-bungarotoxin and similar snake alpha-neurotoxins also targeting alpha7 nAChR.

13 ription of the contacts between a prototypic alpha-neurotoxin and its cognate recognition sequence.

14 olved in the binding interaction on both the alpha-neurotoxin and the receptor interface.

15 While the alpha-neurotoxins are monomeric, the kappa-neurotoxins o

16 alpha-Neurotoxins are potent inhibitors of the nicotinic

17 The alpha-neurotoxins are three-fingered peptide toxins that

18 igate whether the alpha18-mer can bind other alpha-neurotoxins besides alpha-bungarotoxin, we designe

19 alpha-Neurotoxins bind with high affinity to alpha-gamma

20 ica mossambica (NmmI) that, similar to other alpha-neurotoxins, binds with high affinity to alphagamm

21 interaction, we examined the flexibility of alpha-neurotoxin bound to the acetylcholine-binding prot

22 alpha-Neurotoxins constitute a large family of polypepti

23 Like the kappa-neurotoxins, the long alpha-neurotoxins contain the same five conserved disulf

24 otoxins readily dimerize in solution and the alpha-neurotoxins do not and also suggest that there is

25 domain and tested the effect of short-chain alpha-neurotoxin erabutoxin-a (ETX-a) from the Erabu sea

26 luding two residues conserved throughout the alpha-neurotoxin family (K27 and R33), resulted in subst

27 Amino acid variants of alpha-neurotoxin from N. mossambica mossambica at positi

28 genesis had identified three residues on the alpha-neurotoxin from Naja mossambica mossambica (Lys27,

29 We report here on a short alpha-neurotoxin from Naja mossambica mossambica (NmmI)

30 Because the alpha-neurotoxin from Naja mossambica mossambica I shows

31 The three-fingered alpha-neurotoxins have played a pivotal role in elucidat

32 al resistance against conspecific long-chain alpha-neurotoxins in Elapidae snakes also interfere with

33 pha-conotoxin ImI and a chimeric Naja oxiana alpha-neurotoxin indicating that the major role in alpha

34 that only one face of the second loop of the alpha-neurotoxin is immobilized significantly by its bin

35 The results indicate that bound alpha-neurotoxin is not rigidly oriented on the surface

36 ited by some other three-finger toxins, long alpha-neurotoxin Ls III and nonconventional toxin WTX.

37 g occurs in millisecond time frames, and the alpha-neurotoxins may induce a distinct conformational s

38 To advance our understanding of the alpha-neurotoxin-nAChR interaction, we examined the flex

39 Using a recombinant DNA-derived alpha-neurotoxin (Naja mossambica mossambica, NmmI) and

40 e conserved disulfide bonds, while the short alpha-neurotoxins only contain four of the five.

41 A model describing alpha-neurotoxin resistance in Elapidae snakes is presen

42 Phylogenetic analysis of alpha-neurotoxin resistance suggests that alpha-neurotox

43 of alpha-neurotoxin resistance suggests that alpha-neurotoxin-resistant nAChR evolved first, which pe

44 his effect correlates with the variations in alpha-neurotoxin sensitivity of different species and, i

45 -Bungarotoxin is structurally related to the alpha-neurotoxins, such as alpha-bungarotoxin derived fr

46 uorescent conjugate of fasciculin 2, a snake alpha-neurotoxin that tightly binds to the catalytic sub

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