ライフサイエンスコーパス: soluble NSF attachment protein

1 es not depend on the presence of alpha-SNAP (soluble NSF-attachment protein).

2 sitive factor), working together with SNAPs (soluble NSF attachment proteins).

3 yntaxin, an effect that was rescued by alpha-soluble NSF attachment protein.

4 The soluble NSF attachment protein 25 (SNAP-25) homologue SE

5 ated 25-kDa protein (SNAP-25), n-sec1, alpha soluble NSF attachment protein (alpha SNAP), and synapto

6 e factor (NSF) and its adaptor protein alpha-soluble NSF attachment protein (alpha-SNAP) sustain memb

7 sicular transport machinery component, alpha soluble NSF attachment protein (alpha-SNAP), occurring d

8 ted N-ethylmaleimide-sensitive factor, alpha-soluble NSF attachment protein (alpha-SNAP), synaptosome

9 s established that syntaxin 6 binds to alpha-soluble NSF attachment protein (alpha-SNAP).

10 tosis-associated protein (p115/TAP), and the soluble NSF attachment proteins (alpha- and, gamma-SNAP)

11 ide-sensitive fusion protein [NSF]), Sec17p (soluble NSF attachment protein [alpha-SNAP]), and typica

12 NARE complexes that are dissociated by alpha-soluble NSF attachment protein and NSF.

13 tions contain complexes that comprise beside soluble NSF attachment proteins and SNAREs (soluble NSF

14 ), vesicle trafficking (e.g., two alpha-type soluble NSF attachment proteins), and other, unknown con

15 AP receptor (SNARE, where SNAP is defined as soluble NSF attachment protein, and NSF is defined as N-

16 The two SNAPs (soluble NSF attachment proteins) differ by only five ami

17 factor) and the adaptor protein alpha-SNAP (soluble NSF attachment protein) disassemble all SNARE co

18 mide sensitive factor), together with SNAPs (soluble NSF attachment protein), disassembles the SNARE

19 on of an amino acid transporter and an alpha soluble NSF attachment protein gene specifically in sync

20 xpression analyses that identified the alpha soluble NSF attachment protein (Gm-alpha-SNAP) resistanc

21 The role of alpha/beta-SNAP (Soluble NSF Attachment Protein) in vesicular trafficking

22 n intracellular trafficking by disassembling soluble NSF attachment protein receptor (SNARE ) complex

23 Physiologically, alpha-synuclein chaperones soluble NSF attachment protein receptor (SNARE) complex

24 We show in human cells that a soluble NSF attachment protein receptor (SNARE) complex

25 Understanding the fundamental role of soluble NSF attachment protein receptor (SNARE) complexe

26 ustain membrane trafficking by disassembling soluble NSF attachment protein receptor (SNARE) complexe

27 NO inhibits NSF disassembly of soluble NSF attachment protein receptor (SNARE) complexe

28 The function of synaptotagmin-1 (syt-1):soluble NSF attachment protein receptor (SNARE) interact

29 rate that Bet1p plays a role in potentiating soluble NSF attachment protein receptor (SNARE) interact

30 hondria have not been shown to use canonical soluble NSF attachment protein receptor (SNARE) machiner

31 The ER/Golgi soluble NSF attachment protein receptor (SNARE) membrin,

32 sis by interacting with a complex containing soluble NSF attachment protein receptor (SNARE) molecule

33 shown that platelet secretion is mediated by Soluble NSF Attachment Protein Receptor (SNARE) proteins

34 The functional trafficking steps used by soluble NSF attachment protein receptor (SNARE) proteins

35 igen competition indicated a requirement for soluble NSF attachment protein receptor (SNARE) proteins

36 Soluble NSF attachment protein receptor (SNARE) proteins

37 es (GWAS) have linked genes encoding several soluble NSF attachment protein receptor (SNARE) regulato

38 At this concentration of PI 4,5-P(2) soluble NSF attachment protein receptor (SNARE)-dependen

39 interactions with lipid bilayers in Rab- and soluble NSF attachment protein receptor (SNARE)-dependen

40 Neurotransmission is achieved by soluble NSF attachment protein receptor (SNARE)-driven f

41 Defects in soluble NSF attachment protein receptor (SNARE)-mediated

42 block the packaging of Yip1p, Yif1p, or the soluble NSF attachment protein receptor (SNAREs) into ve

43 cription, giving rise to two target-membrane soluble NSF attachment protein receptor (t-SNARE) isofor

44 ires the interaction of a vesicle-associated soluble NSF attachment protein receptor (v-SNARE) on tra

45 presynaptic membrane through formation of a soluble NSF attachment protein receptor complex (SNARE)

46 denosine triphosphate and to disassemble the soluble NSF attachment protein receptor complex.

47 n the motor protein Myosin Vb (Myo5B) or the soluble NSF attachment protein receptor Syntaxin 3 (Stx3

48 the coiled coil domain-containing Q-SNARE (Q-soluble NSF attachment protein receptor) protein syntaxi

49 ific interaction of HOPS with certain SNARE (soluble NSF attachment protein receptor) proteins ensure

50 xocytosis by cleaving their cytosolic SNARE (soluble NSF attachment protein receptor) substrates.

51 soluble NSF attachment proteins and SNAREs (soluble NSF attachment protein receptor), rab 5, dynamin

52 ever, this process involved formation of new soluble NSF-attachment protein receptor (SNARE) complexe

53 ocytosis is mediated by assemblies of SNARE (soluble NSF-attachment protein receptor) and SM (Sec1/Mu

54 dent mechanism that requires a unique SNARE (soluble NSF-attachment protein receptor)-dependent fusio

55 Munc18-1 and soluble NSF attachment protein receptors (SNAREs) are cr

56 ions between synaptotagmin-1 (syt-1) and the soluble NSF attachment protein receptors (SNAREs) are re

57 Soluble NSF attachment protein receptors (SNAREs) are th

58 Soluble NSF attachment protein receptors (SNAREs) are ty

59 Release of granular cargo is mediated by soluble NSF attachment protein receptors (SNAREs), but d

60 and fusion is the pairing of SNARE proteins (soluble NSF attachment protein receptors) associated wit

61 F), an ATPase that disassembles complexes of soluble NSF attachment protein receptors.

62 unc18-like proteins) and SNARE proteins (for soluble NSF-attachment protein receptors) are essential

63 SNAREs (soluble NSF-attachment protein receptors) are generally

64 ), we find that yeast vacuolar SNAREs (SNAP [Soluble NSF attachment protein] Receptors) increase the

65 /or disassembly with dominant-negative alpha-soluble NSF attachment protein (SNAP) also inhibited tet

66 N-ethylmaleimide-sensitive factor (NSF) and soluble NSF attachment protein (SNAP) are cytosolic fact

67 imide-sensitive fusion protein 2 (dNSF2) and soluble NSF attachment protein (Snap) as strong genetic

68 ng through its binding to and disassembly of soluble NSF attachment protein (SNAP) receptor (SNARE) c

69 lmaleimide-sensitive factor) that rearranges soluble NSF attachment protein (SNAP) receptor (SNARE) p

70 as N-ethylmaleimide-sensitive factor (NSF), soluble NSF attachment protein (SNAP), SNAP receptors (S

71 Importantly, alpha-soluble NSF attachment protein (SNAP), the adaptor prote

72 ng the plasma membrane SNAREs syntaxin-1 and soluble NSF attachment protein (SNAP)-25.

73 system with syntaxin-1A as bait, we isolated soluble NSF attachment protein (SNAP)-29 from a human br

74 -ethylmaleimide-sensitive factor (NSF)-alpha soluble NSF attachment protein (SNAP)-SNAP receptor (SNA

75 RH (R385A and R388A) did not effect basal or soluble NSF attachment protein (SNAP)-stimulated ATPase

76 the ATPase activity of NSF stimulated by the soluble NSF attachment protein (SNAP).

77 In this study, the Soluble NSF-Attachment Protein (SNAP) subfamily of TPR c

78 ty of NSF to interact with alpha-SNAP.SNARE (soluble NSF attachment protein-SNAP receptor) complex, s

79 N-Ethylmaleimide-sensitive factor (NSF), soluble NSF attachment proteins (SNAPs), and SNAP recept

80 chemical studies have demonstrated that NSF, soluble NSF attachment proteins (SNAPs), and SNAP recept

81 hylmaleimide-sensitive fusion protein (NSF), soluble NSF attachment proteins (SNAPs), and SNAREs (SNA

82 of N-ethylmaleimide-sensitive factor (NSF), soluble NSF attachment proteins (SNAPs), and SNAREs in s

83 ive fusion protein (NSF) and alpha- and beta-soluble NSF attachment proteins (SNAPs), as well as dend

84 imide-sensitive fusion protein (NSF/Sec18p), soluble NSF attachment proteins (SNAPs/Sec17p) and SNAP

85 NSF with alpha-SNAP (soluble NSF attachment protein) were required for ATP-de