8.A.10.3.3 KCNE3 or MinK-related peptide 2 of 103 aas with 1 C-terminal TMS. It modulates the gating kinetics and enhances stability of the channel
complex. It assembles with KCNB1 and modulates its gating characteristics of
the delayed rectifier voltage-dependent response (McCrossan et al. 2003). It can associate
with KCNC4/Kv3.4 to form the subthreshold voltage-gated
potassium channel in skeletal muscle and establish the resting
membrane potential in muscle cells. Its association with KCNQ1/KCLQT1
may form the intestinal cAMP-stimulated potassium channel involved in
chloride secretion that produces a current with nearly instantaneous
activation with a linear current-voltage relationship (Schroeder et al. 2000). Campbell et al. 2022 provided guidelines for detailed structural studies of KCNE3 in a native membrane environment, comparing lipid bilayer results to the isotropic bicelle structure and to the KCNQ1-bound cryo-EM structure. It has been implicated in autism spectrum disease (Ben-Mahmoud et al. 2024).
|
Accession Number: | Q9Y6H6 |
Protein Name: | Potassium voltage-gated channel subfamily E member 3 |
Length: | 103 |
Molecular Weight: | 11710.00 |
Species: | Homo sapiens (Human) [9606] |
Number of TMSs: | 1 |
Location1 / Topology2 / Orientation3: |
Cell membrane1 / Single-pass type I membrane protein2 |
Substrate |
|
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1: METTNGTETW YESLHAVLKA LNATLHSNLL CRPGPGLGPD NQTEERRASL PGRDDNSYMY
61: ILFVMFLFAV TVGSLILGYT RSRKVDKRSD PYHVYIKNRV SMI