ライフサイエンスコーパス: Shaker potassium channel

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1 s to evaluate the resting-state model of the Shaker potassium channel.

2 ative to the pore domain in the prototypical Shaker potassium channel.

3 ll the K(v)AP model describes the Drosophila Shaker potassium channel.

4 udied the structure of the C terminus of the Shaker potassium channel.

5 to fit a series of gating currents from the Shaker potassium channel.

6 e S6 helices forms a mechanical gate for the Shaker potassium channel.

7 equence comprising residues A355-I384 in the Shaker potassium channel.

8 d these two issues, using both the Kv2.1 and Shaker potassium channels.

9 single cysteines into the S4 segment of the Shaker potassium channel and expressed the mutants in Xe

10 dy the binding process of kappa-PVIIA to the Shaker potassium channel and the structure of the result

11 al changes underlying voltage sensing in the Shaker potassium channel, and it is superior at a site t

12 n II (Fas II) cell adhesion molecule and the Shaker potassium channel are localized at the Drosophila

13 nt amplitudes of mammalian voltage-activated Shaker potassium channels are modulated by at least two

14 In this method, proteoliposomes containing Shaker potassium channels are synthesized in vitro and i

15 the crystal structure of the T1 domain of a Shaker potassium channel at 1.55 A resolution.

16 TEA blocks the Shaker potassium channel by interacting with a tyrosine

17 ng the first S4 arginine by histidine in the Shaker potassium channel creates a proton pore when the

18 y transfer a fluorescent based technique, to Shaker potassium channels expressed in live Xenopus oocy

19 When applied to Drosophila Shaker potassium channels expressed in mammalian cells,

20 We found that P/C-type inactivation of Shaker potassium channels expressed in Xenopus oocytes i

21 We have cloned cDNAs for the shaker potassium channel gene from the spiny lobster Pan

22 n of Kv1 channel functions, mutations of the Shaker potassium channel gene in Drosophila and the KCNA

23 The structure of the Shaker potassium channel has been modeled as passing thr

24 or the cell surface expression of functional Shaker potassium channels in Xenopus oocytes.

25 d accord with experimental estimates for the Shaker potassium channel, indicating that the final mode

26 pendent potassium current is mediated by the Shaker potassium channel Kv1.5.

27 In the Shaker potassium channel, mutation of the first arginine

28 of site-specific fluorescent labeling of the Shaker potassium channel protein with voltage clamping,

29 energy transfer to measure distances between Shaker potassium channel subunits at specific residues.

30 sylation on the traffic of the voltage-gated Shaker potassium channel through the secretory pathway o

31 , Lys26) to block K(+) currents carried by a Shaker potassium channel variant.

32 uence of the S4 transmembrane segment of the Shaker potassium channel was determined in methanol, and

33 e role of the S4 region in the activation of Shaker potassium channel was studied by statistical anal

34 m Conus purpurascens venom that inhibits the Shaker potassium channel, was chemically synthesized in

35 By measuring gating currents from the Shaker potassium channel, we demonstrate here that short

36 e pH-dependence of CTX block of a tetrameric Shaker potassium channel with a single copy of a histidi

37 nal changes in three specific regions of the Shaker potassium channel with site-directed fluorescent

38 served Trp434-Asp447 indole hydrogen bond in Shaker potassium channels with a non-hydrogen bonding ho

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