ライフサイエンスコーパス: bacterial adhesin

1 C attachment to the gut by blocking the FimH bacterial adhesin.

2 ough splitting a domain from a Gram-positive bacterial adhesin.

3 cross-links are widespread in Gram-positive bacterial adhesins.

4 ivity that mediates protein glycosylation of bacterial adhesins.

5 ning the carbohydrate binding specificity of bacterial adhesins.

6 ory epithelia or exhibit similarity to known bacterial adhesins.

7 olved in UTI-induced preterm labor involving bacterial adhesins.

8 ink between the enzyme and the expression of bacterial adhesins.

9 s strains lacking expression of pertactin, a bacterial adhesin and vaccine target, are emerging.

10 rface involves specific interactions between bacterial adhesins and adsorbed salivary components.

11 pB) that had amino acid sequence homology to bacterial adhesins and structural homology to bacterial

12 To evaluate the relative contributions of bacterial adhesins and toxins to ciliary binding, we use

13 is a member of a diverse family of predicted bacterial adhesins, and although lacking a high degree o

14 They are also important bacterial adhesins, and nonpiliated mutants of P. aerugi

15 ose encoded protein has characteristics of a bacterial adhesin; and implicated Ace in binding to coll

16 This attachment is facilitated by bacterial adhesins at the cell surface.

17 r hypotheses that some ligands recognized by bacterial adhesins change their compartmentalization and

18 invasion of heart tissue is dependent on the bacterial adhesin choline-binding protein A that binds t

19 h repeat glycoproteins (SRRPs) are important bacterial adhesins conserved in streptococci and staphyl

20 de O-linked to the serine-rich repeat of the bacterial adhesin, Fap1 of Streptococcus parasanguinis.

21 Here we study the bacterial adhesin FimH to address the role of the inacti

22 One example is the bacterial adhesin FimH, where the C-terminal pilin domai

23 nters around FimH antagonists that block the bacterial adhesin FimH, which would otherwise mediate bi

24 ike serine-rich proteins are a new family of bacterial adhesins found in a variety of streptococci an

25 lycoproteins (SRRPs) are a growing family of bacterial adhesins found in many streptococci and staphy

26 s identified 19 genes with homology to known bacterial adhesin genes, virulence genes, genes involved

27 cterized, the interactions of defensins with bacterial adhesins have not.

28 ructural studies on a class of Gram-positive bacterial adhesins have revealed an intramolecular Cys-G

29 ns are mediated through the binding of other bacterial adhesins, in particular the Opa family of oute

30 This study tested the hypothesis that the bacterial adhesin intimin contributes to tissue specific

31 cing (A/E) pattern, which is mediated by the bacterial adhesin intimin.

32 in with similarity to the well-characterized bacterial adhesins intimin and invasin.

33 pathogen recognition receptors detecting the bacterial adhesin invasin (Inv).

34 ulosis internalization is interaction of the bacterial adhesins invasin and YadA with host cell beta1

35 FadA is a unique bacterial adhesin/invasin in that it utilizes its own tw

36 ng this role is lacking, largely because the bacterial adhesins involved in this host-microbe associa

37 Adherence to host epithelium, mediated by bacterial adhesins, is one of the first steps in NTHi co

38 the identification of a yet uncharacterized bacterial adhesin, LabA, which specifically recognizes l

39 ibody-antigen, vascular selectin-ligand, and bacterial adhesin-ligand interactions.

40 is secreted in significant amounts and that bacterial adhesins may have other activities, prompted a

41 Distinct bacterial adhesins may mediate these cooperative interac

42 eukaryotic and bacterial viruses as well as bacterial adhesins might have a similar maturation mecha

43 lt both because it is polyvalent and because bacterial adhesins often recognize more than one type of

44 Thus, bacterial adhesins (or other surface antigens) with the

45 IRF-1 expression depends on the presence of bacterial adhesin, our findings do not preclude the poss

46 Bacterial adhesins play an important role in the coloniz

47 Since these bacterial adhesins recognize their respective glycolipid

48 uggested a proteinaceous nature of potential bacterial adhesin(s) for hTSP-1.

49 However, the bacterial adhesin(s) remain elusive.

50 an E. faecalis sequence, ace, that encodes a bacterial adhesin similar to the collagen binding protei

51 Collectively, these findings establish a new bacterial adhesin structure that has in effect been hija

52 host cells, thus allowing interactions with bacterial adhesins such as intimin.

53 previously discovered a widespread group of bacterial adhesins, termed Multivalent Adhesion Molecule

54 h repeat glycoproteins (SRRPs) are important bacterial adhesins that are conserved in streptococci an

55 sinia adhesin A (YadA) belongs to a class of bacterial adhesins that form trimeric structures.

56 sents a new paradigm for target binding by a bacterial adhesin, the identification of which will info

57 ased at sites of inflammation, and allow the bacterial adhesin to selectively associate with surface-

58 We have developed a mouse model to study the bacterial adhesins which mediate the increased intestina

59 lecules and highlight the first example of a bacterial adhesin with two domains that participate in a

60 y infections initiated by the interaction of bacterial adhesins with carbohydrate receptors can be po

61 is aided by the interaction between numerous bacterial adhesins with components of the extracellular

62 onic acid capsule impedes the interaction of bacterial adhesins with keratinocyte receptors, (iii) mo

63 sruption or modulation of the interaction of bacterial adhesins with LR might engender unexpectedly b