ライフサイエンスコーパス: peptide domain

1 F(GCNt)), or deleting the TM, CT, and fusion peptide domain.

2 nd is directed by a C-terminal 44-amino acid peptide domain.

3 n and flanking CBF1 interact with the fusion peptide domain.

4 nce followed by a positively charged transit peptide domain.

5 runcate the E-cadherin protein in the signal peptide domain.

6 trols or those with inclusion of a scrambled peptide domain.

7 le, synthetic macromolecules and proteins or peptide domains.

8 pon simple mixing and hetero-assembly of the peptide domains.

9 ar matrix (ECM) molecules and their adhesive peptide domains.

10 s that retain the functions of the displayed peptide domains.

11 a unique low energy complex between the two peptide domains.

12 resequences composed of an N-terminal signal peptide domain and a stromal targeting domain containing

13 nslated proteins for transmembrane or signal peptide domains and found that about 40 proteins had one

14 ution of each factor, discuss Tax's critical peptide domains and highlight its post-transcriptional m

15 dulates APP processing was mapped to a seven peptide domain around the second NPXY domain (residues 4

16 contains the viral transmembrane and fusion peptide domains at the same end of the molecule.

17 tein containing seven repeats of the CC43 WW peptide domain (C), and 8-arm star-shaped PEG conjugated

18 One of the peptide domains, composed of 247 amino acids, binds both

19 A peptide domain comprised of amino acid residues 20 throu

20 The FTIR results also show that peptide domains culled from a longer protein do not nece

21 t activation of FPRL1 on human moncytes by a peptide domain derived from HIV-1 gp120 could lead to de

22 leucyl-phenylalamine (fMLF), is activated by peptide domains derived from the human immunodeficiency

23 A synthetic peptide domain, designated F peptide, corresponding to a

24 surface of the ER but lacking a hydrophobic peptide domain, did not accumulate on LDs.

25 rary of 38 variants of the 23-residue fusion peptide domain found at the N-terminus of gp41 glycoprot

26 rt hydrophobic regions referred to as fusion peptide domains (FPDs) at or near the amino terminus of

27 muli-responsive nanostructures produced with peptide domains from the extracellular matrix offer grea

28 agglutinin glycoprotein, known as the fusion peptide domain (HAfp23), is vital to the membrane fusion

29 nd is catalyzed by the binding of the fusion peptide domain (HFP) of the HIV gp41 protein to the host

30 creted, confirming that the predicted signal peptide domain in MAC1 leads to secretion.

31 n approximately 20-residue N-terminal fusion peptide domain in the envelope protein binds to target c

32 e associated with loss of expression of this peptide domain in transgenic mice.

33 nt levels of Tmod in nuclei and then defined peptide domains in Tmod responsible for nuclear import a

34 The shared exon structures and peptide domains, including proton donors, suggest that M

35 HOXD13, we provide evidence for multiple HOX peptide domains interacting with MEIS proteins.

36 oblot analysis, thereby indicating that this peptide domain is exposed on the surface of fimbriae.

37 ochemical properties of the lentivirus lytic peptide domains (LLPs) within the CTT are evidently high

38 ake activity of Mce1A is confined to a small peptide domain located in the core region of the protein

39 -bonded contact becomes possible between the peptide domains located on either side of the unsaturate

40 In particular, the pro-peptide domain (LOX-PP) released from the secreted precu

41 peptide in phagocytes, suggesting that this peptide domain might share a 7-transmembrane, G-protein-

42 rated at cell junctions and contain distinct peptide domains named PDZ1-3, SH3, HOOK, and GUK.

43 sminogen (Pgn) gene, encoding the N-terminal peptide domain (NTP), has been cloned, expressed in Esch

44 Selective replacement of the amorphous peptide domain of a spider silk with poly(ethylene glyco

45 of the interaction of the 16 residue fusion peptide domain of human immunodeficiency virus glycoprot

46 This study was designed to identify the peptide domain of SP-C required for sorting and secretio

47 epresenting the 23-residue N-terminal fusion peptide domain of the HIV-1 gp41 envelope glycoprotein.

48 Our results suggest that this peptide domain of the HIV-1 gp41 may have the potential

49 r an aspartic acid in the hydrophobic signal peptide domain of the protein, underlies the phenotype i

50 The fusion peptide domain of these proteins is important for membra

51 The novel C-terminal peptide domains of MMP-14 are encoded by a single large

52 wo-hybrid assay, in which a library of small peptide domains of T4SS components was screened for inte

53 informational (nucleic acid) and functional (peptide) domains of the resulting joint molecules allows

54 ed to integrins with primary specificity for peptide domains other than Arg-Gly-Asp (RGD); they confi

55 A peptide (domain peptide corresponding to RyR2 residues 2

56 ted to remove the 20 residue C-terminal tail peptide domains present in the wild-type enzyme.

57 In the apratoxins, the N terminus of the peptide domain [(Pro)-(N-Me-Ile)-(N-Me-ala)-(O-Me-Tyr)-(

58 murine peripherin-2 is an amphiphilic fusion peptide domain (residues 312-326) and a highly conserved

59 is evident even in the absence of activation peptide domains responsible for mediating the binding of

60 pe Tmod and Tmod carrying mutations in these peptide domains revealed that Tmod normally traffics thr

61 The MAGUKs are composed of a series of peptide domains that include one or three DHR/PDZs, an S

62 he field has drastically expanded to include peptide domains that were designed through computational

63 ds protein folding by binding to hydrophobic peptide domains through a reversible mechanism directed

64 strategy of exploiting a diverse library of peptide domains to design modular block copolymers enabl

65 lar matrix material by genetically appending peptide domains to the amyloid protein CsgA, the dominan

66 ure of its NH2-terminal tail, an amphipathic peptide domain, to bind, deform, constrict, and destabil

67 tain multiple repeats of WW and proline-rich peptide domains, undergo a sol-gel phase transition upon

68 n and that differences may exist in the MEIS peptide domains utilized by different HOX groups.

69 As the diversity of peptide domains utilized in modular protein engineering

70 aa), each including the 23aa putative signal peptide domain, via a retrovirus system.

71 uences related to SfCPA-FAS indicated that a peptide domain with a putative flavin-binding site is ei

72 Truncation leads to loss of a peptide domain with strong homology to the nucleosome as

73 e demonstrate that the conformation of the T-peptide domain within intact AChE is antigenically indis