Channelpedia

Kir4.2

Description: potassium inwardly-rectifying channel, subfamily J, member 15
Gene: Kcnj15
Alias: Kir4.2, kcnj15, irkk

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Introduction

KCNJ15 (also known as IRKK; KIR1.3; KIR4.2; MGC13584) encodes Kir4.2, an integral membrane protein, potassium inwardly-rectifying channel, subfamily J, member 15. The encoded protein has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Three transcript variants encoding the same protein have been found for this gene.

http://www.ncbi.nlm.nih.gov/gene/3772


Experimental data

Rat Kir4.2 gene in CHO host cells
25 °C
show 35 cells
35 °C
show 26 cells

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Gene

Species NCBI gene ID Chromosome Position
Human 3772 21 77431
Mouse 16516 16 42702
Rat 170847 11 44328

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Transcript

Species NCBI accession Length (nt)
Human NM_170736.3 8407
Mouse NM_001039057.2 5138
Rat NM_133321.2 1486

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Protein Isoforms

Species Uniprot ID Length (aa)
Human Q99712 375
Mouse O88932 375
Rat Q91ZF1 405

Isoforms

Transcript
Length (nt)
Protein
Length (aa)
Variant
Isoform

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Post-Translational Modifications

PTM
Position
Type

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Structure

The residues involved in pHi sensing in Kir channels, such as the Inner Helix acidic residues (Xu [1035] and the ‘RKR triad’ (Schulte [1036], are identical in Kir4.1 and Kir4.2. (Lam [206]

Kir4.2 predicted AlphaFold size

Species Area (Å2) Reference
Human 5808.56 source
Mouse 4358.12 source
Rat 5242.16 source

Methodology for AlphaFold size prediction and disclaimer are available here


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Kinetics

mKir4.2 expressed in Xenopus oocytes displayed a large inwardly rectifying K+ current with inward rectification being intermediate between that of the strong inward rectifier Kir2.1 and the weak inward rectifier Kir1.1. (Pearson [205])


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Expression and Distribution

Kir4.2 channels are expressed in a variety of transporting epithelial within the kidney (Gosset [1028], Lourdel [1029], Shuck [1030], Tucker [1021]), liver (Hill [1031], Glowatzki [1032]), pancreas (Pessias [3]), bladder, stomach and lung (Thiery [1033], and an airway mucosal cell line (Wu [1034]).


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Interaction

Kir4.2 current in Xenopus oocytes can be blocked by Ba+ and Cs+ and weakly blocked by TEA in a voltage-dependent fashion. Intracellular acidification decreased mKir4.2 current in a reversible fashion, while activation of protein kinase C decreased mKir4.2 current in a manner that was not rapidly reversible. Incubation of oocytes in elevated [K+] produced a slowly developing enhancement of current.(Pearson [205])

Kir4.2 can form functional homotetramers, or heterotetramers with Kir5.1. (Pearson [205]) Kir5.1 converts Kir4.2 from a strong to a weak rectifier, rendering it sensitive to pHi, and suggesting that Kir5.1 plays a role in fine-tuning Kir4.2 activity. (Lam [206])


References

205

Pearson WL et al. Expression of a functional Kir4 family inward rectifier K+ channel from a gene cloned from mouse liver.
J. Physiol. (Lond.), 1999 Feb 1 , 514 ( Pt 3) (639-53).

206

Lam HD et al. Modulation of Kir4.2 rectification properties and pHi-sensitive run-down by association with Kir5.1.
Biochim. Biophys. Acta, 2006 Nov , 1758 (1837-45).

Hill CE et al. Cloning, expression, and localization of a rat hepatocyte inwardly rectifying potassium channel.
Am. J. Physiol. Gastrointest. Liver Physiol., 2002 Feb , 282 (G233-40).

Glowatzki E et al. Subunit-dependent assembly of inward-rectifier K+ channels.
Proc. Biol. Sci., 1995 Aug 22 , 261 (251-61).

Wu JV et al. An inwardly rectifying potassium channel in apical membrane of Calu-3 cells.
J. Biol. Chem., 2004 Nov 5 , 279 (46558-65).

Schulte U et al. pH gating of ROMK (K(ir)1.1) channels: control by an Arg-Lys-Arg triad disrupted in antenatal Bartter syndrome.
Proc. Natl. Acad. Sci. U.S.A., 1999 Dec 21 , 96 (15298-303).


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Credits

To cite this page: [Contributors] Channelpedia https://channelpedia.epfl.ch/wikipages/51/ , accessed on 2024 Nov 21



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