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lysyl-isoleucyl-phenylalanyl-methionyl-lysine

Known as: KIFMK, Lys-Ile-Phe-Met-Lys 
 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (2)

OligopeptidesSodium Channel Blockers

Papers overview

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2014
2014
Experimental design-guided development of a stereospecific capillary electrophoresis assay for methionine sulfoxide reductase enzymes using a diastereomeric pentapeptide substrate.
A capillary electrophoresis method has been developed and validated to evaluate the stereospecific activity of recombinant human… Expand
2008
2008
Ryanoids and imperatoxin affect the modulation of cardiac ryanodine receptors by dihydropyridine receptor Peptide A.
Ca(2+)-entry via L-type Ca(2+) channels (DHPR) is known to trigger ryanodine receptor (RyR)-mediated Ca(2+)-release from… Expand
2004
2004
Suppression of insulin signalling by a synthetic peptide KIFMK suggests the cytoplasmic linker between DIII‐S6 and DIV‐S1 as a local anaesthetic binding site on the sodium channel
Acetyl‐KIFMK‐amide (KIFMK) restores fast inactivation to mutant sodium channels having a defective inactivation gate. Its binding… Expand
1999
1999
Block of Brain Sodium Channels by Peptide Mimetics of the Isoleucine, Phenylalanine, and Methionine (IFM) Motif from the Inactivation Gate
Inactivation of sodium channels is thought to be mediated by an inactivation gate formed by the intracellular loop connecting… Expand
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1999
1999
1H-NMR and circular dichroism spectroscopic studies on changes in secondary structures of the sodium channel inactivation gate peptides as caused by the pentapeptide KIFMK.
The pentapeptide KIFMK, which contains three clustered hydrophobic amino acid residues of isoleucine, phenylalanine, and… Expand
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1999
1999
A human muscle Na+ channel mutation in the voltage sensor IV/S4 affects channel block by the pentapeptide KIFMK
1 Whole cell patch clamping of transfected HEK293 cells was used to examine the effects of a pentapeptide (KIFMK) containing the… Expand
Highly Cited
1998
Highly Cited
1998
A Critical Role for the S4-S5 Intracellular Loop in Domain IV of the Sodium Channel α-Subunit in Fast Inactivation*
Na+ channel fast inactivation is thought to involve the closure of an intracellular inactivation gate over the channel pore… Expand
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1998
1998
Kinetic Analysis of Block of Open Sodium Channels by a Peptide Containing the Isoleucine, Phenylalanine, and Methionine (IFM) Motif from the Inactivation Gate
We analyzed the kinetics of interaction between the peptide KIFMK, containing the isoleucine, phen-ylalanine, and methionine (IFM… Expand
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1997
1997
Competition for Binding Between Veratridine and KIFMK: An Open Channel Blocking Peptide of the RIIA Sodium Channel
Abstract. Veratridine, an alkaloid isolated from the rhizome of V. album, binds and slows the inactivation of the brain sodium… Expand
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Highly Cited
1996
Highly Cited
1996
Role of an S4-S5 linker in sodium channel inactivation probed by mutagenesis and a peptide blocker
A pair of conserved methionine residues, located on the cytoplasmic linker between segments S4 and S5 in the fourth domain of… Expand
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