ライフサイエンスコーパス: C-terminal side

1 with a five-membered oxazolone ring on their C-terminal side.

2 e N-terminal side and 150 amino acids on the C-terminal side.

3 e N-terminal side and 150 amino acids on the C-terminal side.

4 ed little specificity for amino acids on the C-terminal side.

5 2+) signals to the catalytic domain from its C-terminal side and the GCAP1 module from the distant N-

6 e A1 domain: Clus1 (N-terminal side), Clus2 (C-terminal side), and double cluster (DC), in both full-

7 Changes in the N- and C-terminal side chains appear to make little difference

8 n for the importance of at least five ligand C-terminal side chains in determining PDZ domain binding

9 nct modes of accommodation for beta-branched C-terminal side chains.

10 1 as well as the flanking 20 residues on the C-terminal side for JAK2 interaction and JAK2-dependent

11 med by three strands (beta1-beta3), with the C-terminal side, formed by two strands (beta4-beta5).

12 be used in pseudo-MS(3) mode to identify the C-terminal side fragments from a complex MALDI-ISD spect

13 The last position on the C-terminal side in which the identity of the amino acids

14 relative to the sequence flanking it on the C-terminal side, may be important for its function.

15 ality, N-terminal side C horizontal lineO to C-terminal side NH.

16 This region lies about 50 amino acids on the C-terminal side of a 30-residue motif previously recogni

17 An-PEP also had the ability to cleave at the C-terminal side of Ala, Glu, Gly, Ser, Lys and Leu.

18 tease that cleaves protein substrates on the C-terminal side of asparagine.

19 of model peptide substrates occurred on the C-terminal side of basic amino acids, and Km for this re

20 IgG hydrolyzed peptide bonds on the C-terminal side of basic amino acids, including a bond l

21 olypeptide (VIP) cleaved this peptide on the C-terminal side of basic residues.

22 ment enriched in aromatic amino acids on the C-terminal side of Cys-739 abolished YFP-NCX1 palmitoyla

23 olypeptide segment farther downstream on the C-terminal side of each trihelix region.

24 rescued by deletion of three leucines at the C-terminal side of its hydrophobic domain; however, dele

25 ar ligand-binding sites being located to the C-terminal side of K82.

26 ionally dominant sites were localized to the C-terminal side of M1.

27 ide (CNBr), which hydrolyzes proteins on the C-terminal side of methionine residues.

28 nfirmed An-PEP's cleavage preference for the C-terminal side of Pro and also confirmed that An-PEP ha

29 This analysis confirmed cleavage at the C-terminal side of Pro residues.

30 decreases considerably at amide bonds on the C-terminal side of Pro.

31 protease, which cleaves oligopeptides at the C-terminal side of proline residues and constitutes an i

32 07-Gly-811) is short distance element on the C-terminal side of Site 2 PXXP, which might contact a gr

33 monstrate that another region located on the C-terminal side of TAND2 (82-139 aa) can also bind to TB

34 -barrel motif with a binding cleft along the C-terminal side of the beta-barrel.

35 he cleavage between Arg-51 and Gln-52 on the C-terminal side of the DNA-binding domain.

36 Phe(15) and residues at the C-terminal side of the first alpha-helix (helix H1) occu

37 One structure has a nanobody bound to the C-terminal side of the first nucleotide-binding domain.

38 under conditions that cause cleavage on the C-terminal side of the glycosylation site (N642) in extr

39 h encoded in the amino acid sequences on the C-terminal side of the GPGK crest.

40 The golgin GM130 is thought to bind the C-terminal side of the GRASP domain to recruit GRASP65 o

41 finities for histidines on the N- versus the C-terminal side of the heme.

42 sis leads to high efficiency cleavage at the C-terminal side of the hinge lysine 222 residue, generat

43 oprotease that cleaves a peptide bond on the C-terminal side of the lectin domain.

44 ditional exchange of the two residues on the C-terminal side of the loop (V14A, E15T) had no effect.

45 position P+4, three and four residues on the C-terminal side of the phosphorylatable serine, respecti

46 and the polyproline (poly(P)) domain on the C-terminal side of the poly(Q) domain, heavily influence

47 ashes between Gln and Pro side chains to the C-terminal side of the polyQ segment favor adoption of t

48 es with a leucine at the -2 position; at the C-terminal side of the pY residue, it can recognize two

49 ility to undergo proteolysis by furin at the C-terminal side of the reactive center -Arg355-Ile-Pro-A

50 monstrated that substrate composition to the C-terminal side of the scissile bond as well as interact

51 mbrane simulations, Lys(40), residing at the C-terminal side of the transmembrane helix, is observed

52 Residues K407, K409, K410, and K412 on the C-terminal side of the V3 stem form a second nonconserve

53 binding groups on the N-terminal but not the C-terminal side of the zinc ligand.

54 At the C-terminal side of Tyr(P), TULA-2 generally prefers acid

55 trochemical cleavage of peptide bonds at the C-terminal side of tyrosine and tryptophan generates pep

56 N-terminal sides of proline residues and the C-terminal sides of acidic residues.

57 emonstrate that residues flanking the N- and C-terminal sides of the ETS domain of Elf3 are crucial f

58 was enhanced by sequences on both the N- and C-terminal sides of the RING finger.

59 chondria indicate that regions on the N- and C-terminal sides of the transmembrane regions are seques

60 Selective deletions from the N- and C-terminal sides of the zinc finger domain showed that t

61 e N-terminal side (residues 543-709), or the C-terminal side (residues 592-732), which includes the p