ライフサイエンスコーパス: canavanine

1 r neurons (GRNs) confers responsiveness to L-canavanine.

2 at GR8a contributes to the specificity for L-canavanine.

3 suming plant-derived insecticides, such as L-canavanine.

4 been reported to be required for detecting L-canavanine.

5 r Gr66a resulted in an inability to detect L-canavanine.

6 ress and limited growth in the presence of l-canavanine.

7 ced sensitivity to the toxic arginine analog canavanine.

8 a, can1-100 cells to grow in the presence of canavanine.

9 of upf1Delta, can1-100 cells is inhibited by canavanine.

10 H(2)O(2), ethanol, and the amino acid analog canavanine.

11 es and sensitivity to the arginine analogue, canavanine.

12 type of cpp1(-) mutants, hypersensitivity to canavanine.

13 lps confer resistance to the arginine analog canavanine.

14 salt- or sweet-sensing GRNs to respond to L-canavanine.

15 plied to the separation of L-arginine from L-canavanine (a close analogue of arginine where the termi

16 Delta significantly increased sensitivity to canavanine, a phenotype associated with an rpn10Delta si

17 R98b function together in the detection of L-canavanine, a plant-derived insecticide.

18 he resistance phenotype of an ypq2 mutant to canavanine, a toxic analog of arginine efficiently trans

19 al coaggregation by the arginine homologue l-canavanine, abrogated the increased S. cristatus adhesio

20 nd GR98b in Drosophila S2 cells induces an L-canavanine-activated nonselective cation conductance.

21 Binding of L-canavanine, an analog unable to form hydrogen bonds invo

22 We identified this molecule as l-canavanine, an arginine analog, produced in large quanti

23 When BV2 cells were treated with l-canavanine, an iNOS selective inhibitor, the elevation o

24 d that GRs are essential for responding to L-canavanine and that flies missing DmXR displayed normal

25 ssion of these mutants confers resistance to canavanine and thialysine, phenotypes which are similar

26 persensitive to growth inhibitory effects of canavanine and thialysine, which are analogues of argini

27 d that flies missing DmXR displayed normal L-canavanine avoidance and L-canavanine-evoked action pote

28 ll arginine (Arg) residues in a protein with canavanine (Can), a toxic Arg analogue.

29 onal DnaJ, whereas Lon-dependent turnover of canavanine-containing proteins was slower in dnaJ mutant

30 ependent degradation was affected; abnormal, canavanine-containing proteins were similarly affected.

31 pid degradation of abnormal proteins such as canavanine-containing proteins.

32 isplayed normal L-canavanine avoidance and L-canavanine-evoked action potentials.

33 f these Grs in sweet-sensing GRNs switches L-canavanine from an aversive to an attractive compound.

34 l-Canavanine glycine bromothymol blue (CGB) agar can be us

35 It was positive on canavanine-glycine-bromothymol blue agar.

36 ain of ScRheb are incapable of complementing canavanine hypersensitivity of scrheb disruptant cells.

37 reduced the ability of ScRheb to complement canavanine hypersensitivity of ScRheb-deficient yeast.

38 8a was narrowly required for responding to L-canavanine, in contrast to Gr66a, which was broadly requ

39 One such candidate is L-canavanine, in which an N-methylene of L-arginine is rep

40 L-canavanine-induced action potentials were also abolished

41 ly by incorporation of the amino acid analog canavanine into a model viral Ag.

42 ion of the isosteric, titratable Arg analog, canavanine, into a neurotransmitter receptor in a living

43 ed bitter-sensitive cells failed to detect L-canavanine mixed with sucrose in three different feeding

44 py expression of POL30 (PCNA) suppresses the canavanine mutation rate of all the rad27 alleles, inclu

45 some ((DeltaUbL)rad23) does not suppress the canavanine or cold-sensitive defects of rad23Delta rpn10

46 est that GR8a and GR66a are subunits of an L-canavanine receptor and that GR8a contributes to the spe

47 ee GRs collaborate to produce a functional L-canavanine receptor.

48 ed wild-type frequencies of APOBEC3B-induced canavanine resistance (CanR).

49 type and a high rate of forward mutations to canavanine resistance that result primarily from duplica

50 ning normal cell morphology through Ras1 and canavanine resistance through SpRheb.

51 20-fold increase in frequency of mutation to canavanine-resistance, which was further elevated in a u

52 pear to be due to a bias caused by selecting canavanine resistant isolates in the different HTA1-HTB1

53 process can be detected by the production of canavanine-resistant (can1) mutants among the TRP1 recom

54 We measured the frequency of canavanine-resistant colonies as a measure of nuclear mu

55 isiae in the presence of the arginine analog canavanine results in increased SUMOylation and Slx5-Slx

56 We report here the isolation of canavanine-sensitive derivatives of the previously chara

57 nalysis of P. aeruginosa ADI inhibition by L-canavanine showed that two competing pathways are follow

58 order to demonstrate the generality of the L-canavanine slow substrate inhibition and to distinguish

59 We found that L-canavanine stimulated action potentials in S-type sensil

60 olding stresses caused by the heat shock and canavanine treatment.

61 emental arginine and the arginine antagonist canavanine, we show that arginine availability is a dete

62 ells and inhibits sugar detection) or with L-canavanine (which only activates bitter-sensitive cells)

63 ion intermediate formed in the reaction of L-canavanine with Bacillus cereus ADI partitions between t

64 , a mutant resistant to the toxic effects of canavanine, with low levels of transport activities and