AbstractHanatoxin (HaTx) binds to multiple sites on the surface of the drk1voltage-gated K+ channel and modifies channel gating. We set out to identify channel residues that contribute to form these HaTx binding sites. Chimeras constructed using the drk1and shakerK+ channels suggest that the S3–S4 linker may contain influential residues. Alanine scanning mutagenesis of the region extending from the C terminal end of S3 through S4 identified a number of residues that likely contribute to form the HaTx binding sites. The pore blocker Agitoxin2 and the gating modifier HaTx can simultaneously bind to individual K+ channels. These results suggest that residues near the outer edges of S3 and S4 form the HaTx binding sites and are eccentrically lo...
AbstractThe Kv2.1 voltage-activated K+ channel, a Shab-related K+ channel isolated from rat brain, i...
AbstractThe architecture of the pore-region of a voltage-gated K+ channel, Kv1.3, was probed using f...
Charybdotoxin block of a Shaker K+ channel was studied in Xenopus oocyte macropatches. Toxin on rate...
AbstractHanatoxin (HaTx) binds to multiple sites on the surface of the drk1voltage-gated K+ channel ...
AbstractWe studied the mechanism by which Hanatoxin (HaTx) inhibits the drk1voltage-gated K+ channel...
Potassium channels are membrane proteins that regulate potassium flux across the cell membrane. They...
AbstractThe structurally well-characterized scorpion toxin Agitoxin2 inhibits ion permeation through...
While S4 is known as the voltage sensor in voltage-gated potassium channels, the carboxyl terminus o...
AbstractIn voltage-activated potassium (Kv) channels, basic residues in S4 enable the voltage-sensin...
AbstractCharybdotoxin, a peptide neurotoxin of known molecular structure, blocks Shaker K+ channels ...
Maurotoxin (MTX) is a potent blocker of human voltage-acti-vated Kv1.2 and intermediate-conductance ...
Hanatoxin 1 (HaTx1) is a polypeptide toxin isolated from spider venoms. HaTx1 inhibits the voltage-g...
Hanatoxin 1 (HaTx1) is a polypeptide toxin isolated from spider venoms. HaTx1 inhibits the voltage-g...
The carboxyl terminus of the S3 segment (S3(C)) in voltage- gated potassium channels was suggested t...
AbstractIn voltage-dependent K+ channels, each of the four identical subunits contributes one pore l...
AbstractThe Kv2.1 voltage-activated K+ channel, a Shab-related K+ channel isolated from rat brain, i...
AbstractThe architecture of the pore-region of a voltage-gated K+ channel, Kv1.3, was probed using f...
Charybdotoxin block of a Shaker K+ channel was studied in Xenopus oocyte macropatches. Toxin on rate...
AbstractHanatoxin (HaTx) binds to multiple sites on the surface of the drk1voltage-gated K+ channel ...
AbstractWe studied the mechanism by which Hanatoxin (HaTx) inhibits the drk1voltage-gated K+ channel...
Potassium channels are membrane proteins that regulate potassium flux across the cell membrane. They...
AbstractThe structurally well-characterized scorpion toxin Agitoxin2 inhibits ion permeation through...
While S4 is known as the voltage sensor in voltage-gated potassium channels, the carboxyl terminus o...
AbstractIn voltage-activated potassium (Kv) channels, basic residues in S4 enable the voltage-sensin...
AbstractCharybdotoxin, a peptide neurotoxin of known molecular structure, blocks Shaker K+ channels ...
Maurotoxin (MTX) is a potent blocker of human voltage-acti-vated Kv1.2 and intermediate-conductance ...
Hanatoxin 1 (HaTx1) is a polypeptide toxin isolated from spider venoms. HaTx1 inhibits the voltage-g...
Hanatoxin 1 (HaTx1) is a polypeptide toxin isolated from spider venoms. HaTx1 inhibits the voltage-g...
The carboxyl terminus of the S3 segment (S3(C)) in voltage- gated potassium channels was suggested t...
AbstractIn voltage-dependent K+ channels, each of the four identical subunits contributes one pore l...
AbstractThe Kv2.1 voltage-activated K+ channel, a Shab-related K+ channel isolated from rat brain, i...
AbstractThe architecture of the pore-region of a voltage-gated K+ channel, Kv1.3, was probed using f...
Charybdotoxin block of a Shaker K+ channel was studied in Xenopus oocyte macropatches. Toxin on rate...