ライフサイエンスコーパス: SNAP receptor

1 integral membrane proteins known as SNAREs (SNAP receptors).

2 NSF attachment proteins (SNAPs), and SNAREs (SNAP receptors) are elements of a conserved molecular ma

3 Rab2, Rab7, and its effector, PLEKHM1; and a SNAP receptor complex consisting of Syntaxin 13, Snap29,

4 can associate with Sec9p in the context of a SNAP receptor complex.

5 leimide-sensitive factor attachment protein (SNAP) receptor complex required for regulated neuroexocy

6 ew light on the mechanisms underlying SNARE (SNAP receptor) complex assembly and disassembly, and sug

7 a-SNAP.SNARE (soluble NSF attachment protein-SNAP receptor) complex, suggesting that only when the D1

8 leimide-sensitive factor attachment protein (SNAP) receptor]-dependent SNAP-23-mediated mechanism.

9 soluble NSF attachment proteins (SNAPs), and SNAP receptors from a 20 S particle.

10 e-sensitive factor (NSF)-attachment protein (SNAP) receptor hypothesis (SNARE hypothesis), interactio

11 Unlike the SNAREs (SNAP receptors), important secretory proteins that are b

12 e-sensitive factor (NSF) attachment protein (SNAP) receptors in the target membrane], proteins that a

13 that alpha-SNAP, a soluble component of the SNAP receptor machinery, facilitates transport from endo

14 e-sensitive factor [NSF] attachment protein [SNAP] receptor) machinery in membrane traffic to the api

15 soluble NSF attachment proteins (SNAPs), and SNAP receptor (neuronal SNARE) complexes form 20 S parti

16 e-sensitive factor [NSF] attachment protein [SNAP] receptors) of the syntaxin family.

17 ting that AtPEP12p does indeed function as a SNAP receptor or SNARE.

18 y through phosphorylation of target membrane SNAP receptor proteins and their binding proteins.

19 factor attachment protein receptor protein (SNAP) receptor) proteins, and this is coupled to cortica

20 SNAP receptors provide a powerful strategy to post-trans

21 nd target membranes, called v- and t-SNAREs (SNAp REceptors), respectively.

22 can function as target membrane and vesicle SNAP receptors, respectively, for insulin-responsive GLU

23 maleimide fusion protein attachment protein (SNAP) receptor) SNAP-25 is not required for nerve growth

24 Platelet membrane extracts possess SNAP receptor (SNARE) activity, suggesting that the clas

25 a membrane requires two classes of molecules-SNAP receptor (SNARE) and Sec1/Munc18 (SM) protein.

26 function by catalyzing the disassembly of a SNAP receptor (SNARE) complex consisting of membrane pro

27 5 kDa) homologue capable of forming a binary SNAP receptor (SNARE) complex with ROR2.

28 SNAP receptor (SNARE) complexes bridge opposing membrane

29 -alpha soluble NSF attachment protein (SNAP)-SNAP receptor (SNARE) complexes, while delivery from the

30 r membrane fusion through binding to cognate SNAP receptor (SNARE) complexes.

31 nt negative Arf1, Rab1a/Rab2 GTPases, or the SNAp REceptor (SNARE) component syntaxin 5, all of which

32 Among several SNAP receptor (SNARE) genes, Drosophila syntaxin 13 (syx

33 sembles the binding of NSF and SNAP with the SNAP receptor (SNARE) membrane fusion apparatus.

34 We propose a model in which binding of SNAP receptor (SNARE) protein coiled-coil domains helps

35 Synaptobrevin-2, a snap receptor (SNARE) protein, participates in this proc

36 SNAP receptor (SNARE) proteins function in intracellular

37 The SNAP receptor (SNARE) proteins syntaxin-1, SNAP-25, and

38 rotein/synaptobrevin are collectively called SNAP receptor (SNARE) proteins, and they catalyze neuron

39 ipates with syntaxin and SNAP-25 in synaptic SNAP receptor (SNARE) ternary complex formation in Hirud

40 SNAP receptor (SNARE)-mediated fusion is regarded as a c

41 ment protein alpha (alpha Snap), involved in SNAP receptor (SNARE)-mediated vesicle fusion in many ce

42 Trans-SNAP receptor (SNARE, where SNAP is defined as soluble N

43 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) complex formation between differe

44 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) complexes formed between the SNAR

45 sassembly of soluble NSF attachment protein (SNAP) receptor (SNARE) complexes.

46 t rearranges soluble NSF attachment protein (SNAP) receptor (SNARE) protein complexes was proposed to

47 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) proteins synaptobrevin 2, syntaxi

48 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) proteins syntaxin-1, SNAP-25, and

49 ne fusion is mediated by complexes formed by SNAP-receptor (SNARE) and Secretory 1 (Sec1)/mammalian u

50 pete with alpha-SNAP for binding to synaptic SNAP receptors (SNAREs) and consequently inhibit disasse

51 d the Vam2/6p complex is bound to cis-paired SNAP receptors (SNAREs) on isolated vacuoles.

52 NSF), soluble NSF attachment protein (SNAP), SNAP receptors (SNAREs), rab-type GTPases, and Sec1p hom

53 typical vesicle (v) and target membrane (t) SNAP receptors (SNAREs).

54 e NSF attachment proteins (SNAPs/Sec17p) and SNAP receptors (SNAREs).

55 leimide-sensitive factor-attachment protein (SNAP) receptors (SNAREs) on the fusion of egg L-alpha-ph

56 e-sensitive factor (NSF) attachment protein (SNAP) receptors (SNAREs) on this process.

57 -sensitive factor adaptor protein receptors (SNAP receptors, SNAREs) mediate fusion between vesicles

58 ired by nature's engineered proteins such as SNAP receptor [soluble N-ethylmale-imide-sensitive facto

59 s, together with the general target membrane SNAP receptor (t-SNARE) protein SNAP-23 appear to make u

60 yces cerevisiae requires two distinct target SNAP receptor (t-SNARE) proteins, Pep12p and Vam3p.

61 lpha-granule release is dependent on vesicle SNAP receptor-target SNAP receptor (vSNARE-tSNARE) inter

62 ein syntaxin 1a (where SNARE is derived from SNAP receptor (the soluble N-ethylmaleimide-sensitive fu

63 y of target (t-SNARE) and vesicle-associated SNAP receptor (v-SNARE) proteins is a critical step for

64 Among the membrane-bound v-SNAP receptor (v-SNARE) proteins, Bos1p is required only

65 is dependent on vesicle SNAP receptor-target SNAP receptor (vSNARE-tSNARE) interactions.

66 ive fusion protein [NSF] attachment protein [SNAP] receptor) with covalently attached lipids.