ライフサイエンスコーパス: aminopeptidase N

1 ding to the 120 kDa Cry1Ac putative receptor aminopeptidase N.

2 ts strongly indicate that mouse p161 is CD13/aminopeptidase N.

3 t p161 is homologous with rat and human CD13/aminopeptidase N.

4 t of aminopeptidase N that is conserved with aminopeptidase Ns.

5 The apical PM proteins aminopeptidase N, 5'nucleotidase, and the polymeric IgA

6 lar characterization of an Anopheles gambiae aminopeptidase N (AgAPN1) as the predominant jacalin tar

7 activity (64.5 +/- 3.5% of control) but not aminopeptidase N, aminopeptidase P, and 5'-nucleotidase

8 The midgut-specific anopheline alanyl aminopeptidase N (AnAPN1) is highly conserved across Ano

9 ide GNGRAHA, a ligand of the surface protein aminopeptidase N and of integrin alphavbeta3.

10 The viruses used the human entry receptor aminopeptidase N and replicated in human hepatoma cells,

11 ch as alpha(v)beta3/alpha(v)beta5 integrins, aminopeptidase N, and aminopeptidase A.

12 t Phe(3) is a key residue for neprilysin and aminopeptidase N (AP-N) ectoenkephalinase inhibition.

13 ced the levels of the AngIV-degrading enzyme aminopeptidase N (AP-N).

14 angiotensin-I-converting enzyme (ACE I) and aminopeptidase N (AP-N).

15 Tumor cell surface aminopeptidase N (APN or CD13) has two puzzling function

16 activity of specific neuropeptidases, namely aminopeptidase N (APN) and neutral endopeptidase 24.11 (

17 Mouse Dmp1 has been shown to activate CD13/aminopeptidase N (APN) and p19ARF gene expression via bi

18 Here we identify membrane alanyl aminopeptidase N (APN) as a receptor for pea enation mos

19 nsmissible gastroenteritis virus (TGEV), use aminopeptidase N (APN) as their cellular receptors.

20 bound purified gypsy moth (Lymantria dispar) aminopeptidase N (APN) biphasically.

21 ation in the Drosophila homolog of the human aminopeptidase N (APN) gene.

22 which belong to the group 1 coronavirus, use aminopeptidase N (APN) of their natural host and feline

23 Mammalian aminopeptidase N (APN) plays multifunctional roles in ma

24 Further binding assays were performed with aminopeptidase N (APN) purified from L. dispar and M. se

25 and we show that inhibition of cell surface aminopeptidase N (APN) using actinonin, bestatin, or inh

26 Recently, a 100-kDa aminopeptidase N (APN) was isolated from brush border me

27 Aminopeptidase N (APN), a 150-kDa metalloprotease also c

28 of this family that has been well studied is aminopeptidase N (APN), a multifunctional protease known

29 A 106-kDa aminopeptidase N (APN), called AgAPN2, was previously id

30 A nonspecific exopeptidase, aminopeptidase N (APN), is inhibited sequence-specifical

31 tosis of the single-spanning apical resident aminopeptidase N (APN).

32 Aminopeptidase N (APN, CD13; EC 3.4.11.2) is a transmemb

33 ptidases, neprilysin (NEP, EC 3.4.24.11) and aminopeptidase N (APN, EC 3.4.11.2).

34 for the NGR peptides in tumor vasculature is aminopeptidase N (APN; also called CD13).

35 The metalloprotease aminopeptidase N (APN; CD13) is often overexpressed in t

36 of natural promoters revealed that the CD13/aminopeptidase N (APN; EC 3.4.11.2) promoter could bind

37 d with differential alteration of two midgut aminopeptidases N, APN1 and APN6, conferred by a trans-r

38 Lepidopteran midgut aminopeptidases N (APNs) are phylogenetically divided in

39 nsin-converting enzyme; aminopeptidase A and aminopeptidase n; at(1); and at(2) receptors were shown

40 cificity of human, pig, and rat orthologs of aminopeptidase N (CD13), a highly conserved cell surface

41 ibitors tested, or by a mAb directed against aminopeptidase N (CD13).

42 CD13/aminopeptidase N (CD13/APN) is a potent regulator of ang

43 The CD13/aminopeptidase N (CD13/APN) metalloprotease is an import

44 The Ets-1- and c-Myb-dependent aminopeptidase N (CD13/APN) promoter and an Ets-1-depend

45 ular adhesion molecule 1 (ICAM-1), anti-LG3, aminopeptidase N, CXCL9, endothelin-1, and gelsolin.

46 We have recently demonstrated that CD13 (aminopeptidase N) expressed by nonmalignant host cells o

47 CD13 (aminopeptidase N) expression in pericytes was determined

48 Aminopeptidase N from Escherichia coli is a M1 class ami

49 PEDV recognizes protein receptor aminopeptidase N from pig and human and sugar coreceptor

50 Human coronavirus HCoV-229E uses human aminopeptidase N (hAPN) as its receptor.

51 d to purified, soluble virus receptor, human aminopeptidase N (hAPN).

52 Human aminopeptidase N (hAPN/hCD13) is a dimeric membrane prot

53 lasma membrane proteins, 5'-nucleotidase and aminopeptidase N in lysosomal vacuoles.

54 EMV binds to a heavily glycosylated receptor aminopeptidase N in the pea aphid gut and is transcytose

55 the aminopeptidase A inhibitor, EC33, or the aminopeptidase N inhibitor, PC18.

56 CD13/aminopeptidase N is a negative regulator of mast cell ac

57 CD13/aminopeptidase N is a transmembrane peptidase that is in

58 iensis Cry1Ac toxin to the putative receptor aminopeptidase N is specifically inhibited by N-acetylga

59 we found the receptor for HCoV-229E (CD13 or aminopeptidase N) localized mainly to the apical surface

60 r with the lack of receptor functionality of aminopeptidase N proteins might account for some of the

61 tomegalovirus (CMV) infection by human CD13 (aminopeptidase N)-specific antibodies were studied.

62 against partially purified mouse intestinal aminopeptidase N specifically blocked the binding of K-1

63 In this work, aminopeptidase N (TcAPN-I), E-cadherin (TcCad1), and sod

64 d hydrophobic character for the S1 pocket of aminopeptidase N that is conserved with aminopeptidase N

65 s residue methionine 260 in Escherichia coli aminopeptidase N were characterized.

66 f a receptor protein in the aphid gut called aminopeptidase N, which is responsible for entry of the