ライフサイエンスコーパス: membrane fusion protein

1 mediated by the E1 protein, a class II virus membrane fusion protein.

2 mediated by the E1 protein, a class II virus membrane fusion protein.

3 e, which functions as a receptor binding and membrane fusion protein.

4 which is probably derived from an ancestral membrane fusion protein.

5 HAP2 that reveal homology to class II viral membrane fusion proteins.

6 he only feature that E2 shares with class II membrane fusion proteins.

7 are involved in the activation of some virus membrane fusion proteins.

8 ional homology with other well-characterized membrane fusion proteins.

9 f specialized virus envelope proteins termed membrane fusion proteins.

10 s domain has a similar function in different membrane fusion proteins.

11 s a common motif found in many diverse viral membrane-fusion proteins.

12 s in retrovirus, paramyxovirus and filovirus membrane-fusion proteins.

13 dentifying coiled-coil-like regions in viral membrane-fusion proteins.

14 ibed for the haemagglutinin and HIV/SIV gp41 membrane-fusion proteins.

15 ms a cell envelope-spanning complex with the membrane fusion protein AcrA and the outer membrane prot

16 novel classes of EPIs that interact with the membrane fusion protein AcrA, a critical component of th

17 he RND transporter All3143 and the predicted membrane fusion protein All3144, as homologs of E. coli

18 e the cytoplasmic membrane-localized ATPase, membrane fusion protein and outer membrane protein compo

19 in channels tested but necessitated the MexJ membrane fusion protein and the MexK inner membrane RND

20 in order to understand the functionality of membrane fusion proteins and to define key parameters in

21 mary active transporter (IMP), a periplasmic membrane fusion protein, and an outer membrane channel.

22 a central RND proton-substrate antiporter, a membrane fusion protein, and an outer membrane factor.

23 I) associates with AcrA(HI), the periplasmic membrane fusion protein, and the outer membrane channel

24 l, inner membrane transporter; a periplasmic membrane fusion protein; and a beta-barrel, outer membra

25 r membrane, substrate-binding transporter; a membrane fusion protein; and an outer-membrane-anchored

26 poyl/biotin swinging arm domain in bacterial membrane fusion proteins; and a DH domain in the yeast B

27 that several members of the SNARE family of membrane fusion proteins are expressed in TALs.

28 are set apart from other viral and cellular membrane fusion proteins by their extensively palmitoyla

29 n, vesicle accumulation at lesion sites, and membrane fusion proteins; Ca(2+) influx also initiates c

30 A family of membrane fusion proteins called SNAREs, which are presen

31 the outer membrane component, TolC, and the membrane fusion protein component, AcrA, of the major an

32 4830-4919)-GFP, were localized to the plasma membrane; fusion proteins containing the fourth transmem

33 , we found that purified MacA, a periplasmic membrane fusion protein, contains one tightly bound roug

34 the inner membrane transporter CusA and the membrane fusion protein CusB of the CusCBA efflux system

35 both the inner-membrane transporter CusA and membrane fusion protein CusB of the CusCBA tripartite ef

36 r edges to establish a "switch" role for the membrane fusion protein CusB.

37 ) proteins comprise a unique family of viral membrane fusion proteins dedicated to inducing cell-cell

38 H dissociates the E2/E1 dimer, releasing the membrane fusion protein E1.

39 rusion of periplasmic substrate bypasses the membrane fusion protein, enters the RND-transporter dire

40 YegN and YegO produce a complex(es) with the membrane fusion protein family member YegM and pump out

41 E possesses features similar to those of the membrane fusion protein family that facilitates the pass

42 jacent genes yhcQ, encoding a protein of the membrane fusion protein family, and yhcR, encoding a sma

43 owed that AcrA, a periplasmic protein of the membrane fusion protein family, could function with at l

44 As a member of the membrane fusion protein family, CvaA is supposed to form

45 by deletion of mitochondrial outer or inner membrane fusion proteins (Fzo1p or Mgm1p) leads to decre

46 logy with viral trimeric coiled-coil class I membrane fusion proteins, gp26 may represent the membran

47 A prevailing model for virus membrane fusion proteins has been that the hydrophobic f

48 he coiled-coil motif occurs in several viral membrane-fusion proteins, including HIV-1 gp41 and influ

49 l architecture resembles several other viral membrane-fusion proteins, including those from HIV and i

50 itch model requires substrate binding to the membrane fusion protein, inducing a conformational chang

51 Annexin 7, a Ca(2+)/GTP-activated membrane fusion protein, is preferentially phosphorylate

52 ncreased expression of AcrA, the periplasmic membrane fusion protein, is toxic only in cells lacking

53 eukaryotic cells and has been linked to the membrane-fusion proteins known as soluble N-ethylmaleimi

54 The membrane fusion protein MacA not only stabilizes the tri

55 to a binding domain for interaction with the membrane fusion protein MacA.

56 or MF; periplasmic proteins belonging to the membrane fusion protein (MFP) family; and outer membrane

57 These systems contain a periplasmic membrane fusion protein (MFP) that is critical for subst

58 orter, an outer-membrane factor (OMF), and a membrane fusion protein (MFP) that spans the periplasmic

59 AmeA and AmeB show high homology to membrane fusion proteins (MFP) and RND-type transporters

60 Periplasmic membrane fusion proteins (MFPs) are essential components

61 Periplasmic membrane fusion proteins (MFPs) are essential components

62 rters function in complexes with periplasmic membrane fusion proteins (MFPs) that enable antibiotic e

63 his putative RND pump contains two predicted membrane fusion proteins (MFPs), ZrpA and ZrpD.

64 Deletion of the membrane fusion protein MtrC rendered H. ducreyi more se

65 of the outer membrane component MtrE and the membrane fusion protein MtrC, obtained by a combination

66 MtrE, which are connected by the periplasmic membrane fusion protein MtrC.

67 uires adenosine triphosphate and the general membrane fusion protein, N-ethylmaleimide sensitive fact

68 airpins motif, predicts these regions in the membrane fusion protein of the Visna virus.

69 oted in the regulatory domain of synexin the membrane fusion protein of Xenopus laevis.

70 Viral membrane fusion proteins of class I are trimers in which

71 resembles the conformational transitions of membrane fusion proteins of enveloped viruses.

72 es encode homologues of ABC transporters and membrane fusion proteins of Type I secretion systems, re

73 nfected with HIV-1 and therefore had the HIV membrane fusion protein on their surface.

74 The mammalian mitochondrial inner membrane fusion protein OPA1 is controlled by complex pa

75 When the inner membrane fusion protein Opa1 level was lowered or was gr

76 binding transporter (or pump); a periplasmic membrane fusion protein (or adaptor); and an outer-membr

77 The fusion peptides of viral membrane fusion proteins play a key role in the mechanis

78 Baculovirus GP64 is a low-pH-dependent membrane fusion protein required for virus entry and cel

79 ologically different to that mediated by the membrane fusion proteins, SNAREs, as initial fusion is b

80 Structural studies of viral membrane fusion proteins suggest that a "trimer-of-hairp

81 In this complex, AcrA is a periplasmic membrane fusion protein that establishes a functional co

82 polyhedrovirus (AcMNPV) is a class III viral membrane fusion protein that is triggered by low pH duri

83 In this complex, MacA is the periplasmic membrane fusion protein that stimulates the activity of

84 y hydrophobic segments of viral and nonviral membrane fusion proteins that enable these proteins to f

85 It is not known how membrane fusion proteins that function at neutral pH, fo

86 shuttling of periplasmic substrate from the membrane fusion protein to the RND transporter and furth

87 the outer membrane protein TolC and cognate membrane fusion proteins to form tripartite transperipla

88 ly P. aeruginosa RND pump which contains two membrane fusion proteins, TriA and TriB, and both are re

89 nthesized, and the soluble core of the Visna membrane fusion protein was reconstituted in solution.

90 ce lacking specific vesicle-associated SNARE membrane fusion proteins, we found that VAMP-8-deficient

91 functions together with MacA, a periplasmic membrane fusion protein, which stimulates MacB ATPase.

92 ter PRV infection due to the action of viral membrane fusion proteins, yet it is unclear if such acti

93 plex from Bacillus subtilis, where YknX is a membrane fusion protein, YknY is an ATPase, and YknZ is