ライフサイエンスコーパス: hydrophilic region

1 l catalytic domain, linked by a nonconserved hydrophilic region.

2 of aromatase, whose signal anchor follows a hydrophilic region.

3 nly if the aqueous liquid first occupies the hydrophilic region.

4 main and most of the contiguous proline-rich hydrophilic region.

5 ed into two groups of six by a large charged hydrophilic region.

6 ibodies contained arginine mutations in more hydrophilic regions.

7 ns that contain many FG-repeats separated by hydrophilic regions.

8 annel systems with patterned hydrophobic and hydrophilic regions.

9 creases whereas the converse applies to more hydrophilic regions.

10 etrate the bilayer, allowing the intervening hydrophilic region (334-398) to cross the membrane.

11 In the major hydrophilic region, 56.5% strains were wild type or with

12 TIG3 encodes an N-terminal hydrophilic region (amino acids 1-135) and a C-terminal

13 ropionic acid tails point outward toward the hydrophilic region and extend into the solvent.

14 ermally patterned arrays adhered only to the hydrophilic regions and was repelled from the hydrophobi

15 According to this model most of the Ste14p hydrophilic regions are located in the cytosol.

16 Epitope-mapping studies revealed that these hydrophilic regions are located on one side of the prote

17 nist, and ribose moiety was coordinated in a hydrophilic region, as previously predicted based on mod

18 Yop1p is a membrane protein with a hydrophilic region at its N terminus through which it in

19 amino acids of p22phox are required, as is a hydrophilic region between amino acids 65 and 90.

20 Their integration allowed the hydrophilic region between the hydrophobic domains (354-

21 lH protein, including almost all of the long hydrophilic region C-terminal to the transmembrane domai

22 21 and G37-A42 preceding fibril formation in hydrophilic region E22-A30.

23 ophobic region being larger than that of the hydrophilic region, exhibited strong interleukin-6 (IL-6

24 integrated into a detergent micelle and its hydrophilic region extending outward from the micelle su

25 utinin, monoclonal antibody Mab1) at various hydrophilic regions flanking each of its predicted TMDs,

26 teria), type II (CAXs with a long N-terminus hydrophilic region, found in fungi, Dictyostelium, and l

27 ressing the solvent-exposed area adjacent to hydrophilic region II, conserved a high activity of the

28 ace normal, with one end protruding past the hydrophilic region into the fluid subphase and the other

29 ly, we have shown that the AtNHX1 C-terminal hydrophilic region localized in the vacuolar lumen plays

30 ences in locations of water molecules in the hydrophilic region near guest molecules.

31 ules interact with the phosphopeptide in the hydrophilic region of the lattice.

32 ugh both ions are incorporated deep into the hydrophilic region of the membrane, they have different

33 ere the donor fluorophore is attached to the hydrophilic region of the molecule.

34 no-acid peptide corresponding to an internal hydrophilic region of the predicted amino acid sequence

35 91 from the N terminus, corresponding to the hydrophilic region of the protein.

36 interactions occurring predominantly in the hydrophilic region of the proteins, external to the lipi

37 ncy of amino acid substitutions in the major hydrophilic region of the small surface protein (S prote

38 ly, we constructed tim23N, encoding only the hydrophilic region of Tim23p, and tim23C, encoding only

39 ular characterization of the hydrophobic and hydrophilic regions of AOT at the different oil-water in

40 HFAD, ALEAYA, and THEGGQ) are present in the hydrophilic regions of Asp f 2.

41 Eight insertions mapping to distinct hydrophilic regions of MalG permitted either assembly or

42 nts contain insertions in only two different hydrophilic regions of MalG, consistent with the notion

43 ngle amino acid changes in each of the three hydrophilic regions of PEN-2 to generate N-linked glycos

44 of nine peptides that constitute most of the hydrophilic regions of rhodopsin, only one, consisting o

45 Evidence that several different hydrophilic regions of the amino-terminal region of CD14

46 we used alanine mutagenesis to identify two hydrophilic regions of the E1 DNA binding domain (E1DBD)

47 ing hemagglutinin (HA) tags in its predicted hydrophilic regions of the MSD.

48 d, while maintaining solubility owing to the hydrophilic regions of the protein interspersed among th

49 We found that the hydrophilic regions of the Sulfs were essential for endo

50 Nonconservative replacements occurred in hydrophilic regions outside of domains previously implic

51 by an increased affinity for adsorption onto hydrophilic regions relative to the surrounding hydropho

52 demonstrate that a segment of the N-terminal hydrophilic region targets the centrosome.

53 has six putative transmembrane domains and a hydrophilic region that contains a phosphatase motif req

54 le for macrophage activation and an external hydrophilic region that contains the selective lipoprote

55 These two hydrophobic domains flank a large hydrophilic region that shows extensive homology with ot

56 nding site on RyR1 most likely consists of a hydrophilic region to interact with the 1-hydroxyl as we

57 rocedures and patterned into hydrophobic and hydrophilic regions using self-assembled monolayers (SAM

58 extended hydrophobic pocket and an adjacent hydrophilic region, where hydrogen-bonding interactions

59 onstraining hydrophobic pocket adjacent to a hydrophilic region, where potential hydrogen-bonding int

60 The two streptococcal sequences differ in a hydrophilic region with 10 tandem repeats of a 20-mer in

61 Two hydrophilic regions with several highly conserved positi

62 emagglutinin tag or the HisT7 tag at various hydrophilic regions within the human ACAT-1 protein and