ライフサイエンスコーパス: self-processing

1 plicitly temporal in nature or as reliant on self-processing.

2 unique to prokaryotes that undergoes limited self-processing.

3 rimental design featuring ISG15-UBP43 fusion self-processing.

4 sition of Glu11, resulting in stimulation of self-processing.

5 In addition to self-processing activity, trans -cleavage reactions were

6 antly correlated with Psi-induced changes in self-processing and decreased aspartate (Asp) content.

7 cific conformational constraints that govern self-processing and demonstrate that considerable rearra

8 mportant for different aspects of memory and self-processing and for modulation of physiologic respon

9 AtSerpin1 blocked AtMC1 self-processing and inhibited AtMC1-mediated cell death.

10 P2d activity concomitant with Ca(2+)-induced self-processing at multiple internal sites was observed.

11 A cleavable junction suitable for self-processing at the normal maturation point of human

12 In self-processing biochemical reactions, a protein or RNA

13 k (DN) has been consistently associated with self-processing but also with autonomic regulation.

14 RPP30) enhanced k(obs) for the RPR-catalyzed self-processing by approximately 100-fold while the othe

15 te that LTQ biogenesis most likely occurs by self-processing chemistry, requiring only the precursor

16 is copper- and O2-dependent, resulting in a self-processing enzyme system.

17 rial membrane, must undergo an autocatalytic self-processing event to gain activity.

18 ases, the post-translation modification is a self-processing event, whereas in others, another proces

19 These repetitive RNAsundergo self-processing, eventually yielding unit length circula

20 coding 40-nt randomized sequences as well as self-processing hammerhead ribozymes.

21 ggest that, in other systems, a slow rate of self-processing has prevented recognition that a reactio

22 novel functional framework for the DN, where self-processing is coupled with physiological monitoring

23 n Saccharomyces cerevisiae, have indicated a self-processing mechanism for 2,4,5-trihydroxyphenylalan

24 ed accumulation of multiple proteins through self processing of a polyprotein [21].

25 ae carrying avirulent gene avrRpt2, and that self-processing of AtMCP2d was also detected in wild-typ

26 >O acyl shifts initiate the self-processing of other proteins such as inteins and am

27 iological relevance of Ca(2+) dependence and self-processing of plant MCPs remains unclear.

28 Ca(2+)-induced self-processing of recombinant AtMCP2d was found to corr

29 The ribozyme catalyzes self-processing of the 5'- and 3'-ends of a transcribed

30 ential step in this process is the enzymatic self-processing of the UmuD-like proteins.

31 atial imagery, episodic memory retrieval and self-processing operations, namely first-person perspect

32 Furthermore, the NoV polyprotein self-processing order can be altered by interchanging th

33 zes to the cytosol, and its accumulation and self-processing patterns were age-dependent in leaves.

34 linking the heavy and light chains with a 2A self-processing peptide derived from the foot-and-mouth

35 Self-processing polyproteins using the FMDV 2A sequence

36 The molecular mechanism of self-processing, presented here, emphasizes the importan

37 s well as its T. melanosporum ortholog, is a self-processing pro-phospholipase A(2), whose phospholip

38 to a level of 4 x 10(4) copies per cell, and self-processing proceeded to an extent of >75% within ce

39 Rolling circle transcription followed by self-processing produced the desired 63 nt ribozyme, whi

40 Comparison of AdoMetDC with other self-processing proteins shows no common structural feat

41 provides insight into the mechanism for the self-processing reaction and provides evidence for the m

42 ence for the mechanism for simulation of the self-processing reaction by putrescine.

43 e first example of a mutation in a regulated self-processing reaction that impairs the rate of self-p

44 The role of Ser55, His68, and Cys83 in the self-processing reaction was investigated through site-d

45 ed by the ribozyme-containing product of the self-processing reaction, and by the ribozyme linked to

46 ed kinetic isotope effects (KIEs) on the GFP self-processing reaction.

47 at may interfere with the topa quinone (TPQ) self-processing reaction.

48 vity of a number of proteins is regulated by self-processing reactions.

49 self-association depends on p62/SQSTM1, its self-processing requires the autophagosomal membrane.

50 in a cellular environment, and indicate that self-processing ribozyme transcripts may be well suited

51 a circular vector encoding a repeating (non-self-processing) ribozyme is described; the resulting mu

52 the tyrosyl-cysteine (Tyr-Cys) cofactor is a self-processing step requiring only copper and dioxygen.

53 e active catalyst forms in a presteady-state self-processing step that involves oxygenation of the na

54 events that is autonomously executed, termed self-processing synthesis.

55 ows significant similarity to those in other self-processing systems, and suggests that models of the

56 e, that the UmuD-like proteins might undergo self-processing that, in contrast to LexA and lambdaCI,

57 e produced by this system and are capable of self-processing to yield both DSP and PP proteins.

58 Following transient transfection, self-processing transcripts containing active and inacti

59 processing reaction that impairs the rate of self-processing without markedly affecting the stimulate

60 arried such a substitution, discovery of its self-processing would have been difficult; we suggest th