ライフサイエンスコーパス: N-acetylated

1 s of M. leprae peptidoglycan are exclusively N acetylated.

2 copic analysis indicates that Trm1-II-GFP is N-acetylated.

3 terial peptidoglycan are N-glycolylated, not N-acetylated.

4 ns), and its N-terminal residue, alanine, is N-acetylated.

5 zyme that specifically acts on N-sulfated or N-acetylated 6-O-sulfated glucosamines present at the no

6 retical J-couplings were calculated in model N-acetylated aldopyranosides using density functional th

7 ive inhibitor of the NAAG hydrolyzing enzyme N-acetylated alpha-linked acidic dipeptidase (NAAG pepti

8 ubstrate and pharmacologic properties of the N-acetylated alpha-linked acidic dipeptidase (NAALADase)

9 tylaspartylglutamate, has also been known as N-acetylated alpha-linked acidic dipeptidase (NAALADase)

10 The brain enzyme N-acetylated alpha-linked acidic dipeptidase (NAALADase)

11 N-acetylated alpha-linked acidic dipeptidase (NAALADase)

12 hese compounds to inhibit the neuropeptidase N-acetylated alpha-linked acidic dipeptidase (NAALADase)

13 nked acidic dipeptidase-like protein (NLDL), N-acetylated alpha-linked acidic dipeptidase 2 (NAALAD2)

14 s, pig folylpoly-gamma-carboxypeptidase, rat N-acetylated alpha-linked acidic dipeptidase, and human

15 ties of folylpoly-gamma-carboxypeptidase and N-acetylated alpha-linked acidic dipeptidase, while immu

16 lutamate carboxypeptidase II (GCP2 or PSMA), N-acetylated alpha-linked acidic dipeptidase-like protei

17 N-acetylated alpha-linked acidic dipeptidase-like protei

18 es for intestinal folate hydrolase and brain N-acetylated alpha-linked acidic dipeptidase.

19 tate-specific membrane antigen and rat brain N-acetylated alpha-linked acidic dipeptidase.

20 stroke, through the inhibition of NAALADase (N-acetylated-alpha-linked-acidic dipeptidase), an enzyme

21 reason for the higher biological activity of N-acetylated alphaMSH (Act-alphaMSH) compared with that

22 inosine, indole-3-acetate, galactose, and an N-acetylated amino acid (NAA), showed a high sensitivity

23 acids (tryptophan, tyrosine, phenylalanine), N-acetylated amino acids (N-acetyl-tryptophan, N-acetyl-

24 er activity than the wild-type on a range of N-acetylated amino acids.

25 drazine (<10 min), the oligosaccharides were N-acetylated and derivatized with AA in the same reactio

26 ans heparin and heparan sulfate occurring in N-acetylated and N-sulfated forms, and as the unmodified

27 The latter are embedded within N-acetylated and N-sulfated sequences, forming extended

28 Uniquely, sections comprising alternating N-acetylated and N-sulfated units are resistant to the e

29 r of various cysteine sulfinyl ions (intact, N-acetylated, and O-methylated), new members of the gas-

30 xopeptidase that catalyzes the hydrolysis of N-acetylated aspartate-glutamate (NAAG) to N-acetyl aspa

31 [3H]N-acetylbenzidine had a similar ratio of N-acetylated benzidines (N-acetylbenzidine + N',N'-diace

32 The N-acetylated, C-amidated peptide corresponds to the sequ

33 larger (i.e. degrees of polymerization = 8) N-acetylated chitin molecules with a 50% inhibition of i

34 ures were mono- or dihexoses rather than the N-acetylated chitobiosyl core that is characteristic of

35 her anti-HIV activity than the corresponding N-acetylated conjugates against cell-free virus.

36 el, however, was not observed for protonated N-acetylated cysteine sulfinyl radicals (Ac-(SO*)Cys); i

37 N-Acetylated cysteine was also inhibitory, but this inhi

38 ithin non-sulfated sequences of four or more N-acetylated disaccharides.

39 exosite 2 defective mutant, and a synthetic N-acetylated dodecapeptide, Ac-Asn-Gly-Asp-Phe-Glu-Glu-I

40 fated, iduronate-rich domains alternate with N-acetylated domains.

41 nd 10% of the muramic acid residues) was not N-acetylated, explaining the resistance of the peptidogl

42 (S) and 'B-type' (B) conformers, whereas the N-acetylated FAAF also samples a 'wedge' (W) conformer.

43 s acid hydrolysis under conditions where the N-acetylated form is completely labile.

44 Peptide 3 is a cyclic analogue of the N-acetylated form of the heptapeptide C-terminus of the

45 ine (4-amino-4,6-dideoxy- d-mannose), or its N-acetylated form, is one of several dideoxy sugars foun

46 2-(4-Aminophenyl)benzothiazoles 1 and their N-acetylated forms have been converted to C- and N-hydro

47 and free amino groups available on partially N-acetylated fucosamine residues.

48 nd that alpha2-3-linked Neu on chemically de-N-acetylated G(M3) ganglioside resists acid hydrolysis u

49 p to the hexauronic acid that is adjacent to N-acetylated galactosamine.

50 taphylococcal surface of polysaccharide poly-N-acetylated glucosamine (PNAG) by use of human monoclon

51 icylic acid and sodium acetate as well as by N-acetylated glucosamine and galactosamine (GlcNAc and G

52 rtion duplication mutagenesis produced fully N-acetylated glycan and became hypersensitive to exogeno

53 nd a poorly resolved envelope of albumin and N-acetylated glycoprotein resonances.

54 onin T that varied in affinity in the order: N-acetylated > Gly > AlaSer > unacetylated.

55 ation in the order of heparin > N-desulfated N-acetylated heparin > completely desulfated N-sulfated

56 rin > 2-O,3-O-desulfated > or = N-desulfated/N-acetylated heparin > or = carboxyl-reduced heparin > o

57 N-acetylated heparin (NAc-Hep) lacked detectable anticoa

58 ately sulfated adhesin analog, N-desulfated, N-acetylated heparin, was able to compete with chlamydia

59 d N-sulfated heparin > completely desulfated N-acetylated heparin.

60 The N-acetylated hexapeptide WLLLLL (AcWL5) partitions into

61 rms, the secondary amides of peptides and of N-acetylated hexose sugars.

62 GlcN-UA-GlcNAc from HS and from partially de-N-acetylated K5 polysaccharide.

63 Chitosans, beta-1,4-linked partially N-acetylated linear polyglucosamines, are very versatile

64 atalyzing the removal of acetyl groups from -N-acetylated lysine residues of various protein substrat

65 d bactericidal activity were inhibited by de-N-acetylated MBPS and re-N-acetylated MBPS, which indica

66 ere inhibited by de-N-acetylated MBPS and re-N-acetylated MBPS, which indicate that N-propionyl group

67 c acid, and 3-methoxytyramine in addition to N-acetylated metabolites including N-acetyldopamine, N-a

68 a of the imidazole and methionine adducts of N-acetylated microperoxidase 8.

69 occurrence of N-glycolylated, in addition to N-acetylated, muramic acid residues and direct cross-lin

70 id hydroxylase activity and synthesizes only N-acetylated muropeptide precursors.

71 fated S domains interspersed by transitional N-acetylated/N-sulfated domains.

72 A series of N-acetylated, non-alpha, aromatic amino acids was prepar

73 dies were conducted on a subtilisin-digested N-acetylated peptide of the major positional isomer [PEG

74 N-Acetylated peptides AcVYK-amide (AcVYK), AcIVYK-amide

75 investigate this regioselectivity with four N-acetylated peptides as substrates: neurotransmitter me

76 he isolated PDZ10 domain for variable-length N-acetylated peptides from the 5HT2c serotonin receptor

77 is/trans isomerization of the amide bonds of N-acetylated peptoid monomers, dipeptoids, and tripeptoi

78 Binding of N-acetylated Phe-tRNA(Phe), an analog of the initiator f

79 inding mode suitable for interaction with de-N-acetylated PNAG (dPNAG).

80 gh purity and as substrates the partially de-N-acetylated polysaccharide of Escherichia coli K5 strai

81 rotein binding and which are interspersed by N-acetylated, poorly sulfated regions.

82 quires that they possess a free amino group; N-acetylated prenylcysteines and prenyl peptides are not

83 oadipate and tryptophan, to their respective N-acetylated products in several plant species.

84 receptors 1 and 2 on neutrophils, similar to N-acetylated proline-glycine-proline (N-alpha-PGP).

85 d to tetanus toxoid, including completely de-N-acetylated PSA.

86 44 on MIP1alpha and that the interconnecting N-acetylated region is of sufficient length to allow the

87 -rich S-domains separated by a short central N-acetylated region.

88 MAb is a MBPS disaccharide containing one de-N-acetylated residue.

89 consisted of a mixture of N-glycolylated and N-acetylated residues.

90 lting new N termini were N-myristoylated and N-acetylated, respectively.

91 it erythrocytes, which could be inhibited by N-acetylated saccharides.

92 mably single, N-sulfated domain linked to an N-acetylated sequence contiguous with the linkage to cor

93 efined model of the structure of HS in which N-acetylated sequences of four to five disaccharide unit

94 Recombinant (unacetylated) TM2 and N-acetylated striated muscle TM (stTM), long alpha-tropo

95 -fold but totally abolished the activity for N-acetylated substrates, indicating that residue S306 pl

96 e enzyme's specificity for N-formylated over N-acetylated substrates.

97 ntaining monosaccharides, phosphorylated and N-acetylated sugars, polyols, carboxylic acids, nucleoti

98 amines and amides, primary amides, and novel N-acetylated sugars, which together account for nearly 5

99 ns and that the predominant adduct formed is N-acetylated, supporting the concept that monofunctional

100 Non N-acetylated TPMs did not rescue GG-actin polymerization

101 D-glucosamine-alpha-1-phosphate is N-acetylated with [14C]acetate using N-ethoxycarbonyl-2-

102 n of amyloid fibrils formed from full-length N-acetylated WT SOD1 with trypsin, chymotrypsin, or Pron