Protein Details: Potassium voltage-gated channel subfamily G member 4

Protein ID

ICDB_Pro_1317

Protein Name

Potassium voltage-gated channel subfamily G member 4

Gene Name

KCNG4; KCNG3

Organism

Homo sapiens (Human)

Length

519 amino acids

AlphaFoldDB

AF-Q8TDN1-F1-model_v4.pdb

Function

Potassium channel subunit that does not form functional channels by itself. Can form functional heterotetrameric channels with KCNB1; modulates the delayed rectifier voltage-gated potassium channel activation and deactivation rates of KCNB1

Sequence

MPMPSRDGGLHPRHHHYGSHSPWSQLLSSPMETPSIKGLYYRRVRKVGALDASPVDLKKEILINVGGRRYLLPWSTLDRFPLSRLSKLRLCRSYEEIVQLCDDYDEDSQEFFFDRSPSAFGVIVSFLAAGKLVLLQEMCALSFQEELAYWGIEEAHLERCCLRKLLRKLEELEELAKLHREDVLRQQRETRRPASHSSRWGLCMNRLREMVENPQSGLPGKVFACLSILFVATTAVSLCVSTMPDLRAEEDQGECSRKCYYIFIVETICVAWFSLEFCLRFVQAQDKCQFFQGPLNIIDILAISPYYVSLAVSEEPPEDGERPSGSSYLEKVGLVLRVLRALRILYVMRLARHSLGLQTLGLTVRRCTREFGLLLLFLAVAITLFSPLVYVAEKESGRVLEFTSIPASYWWAIISMTTVGYGDMVPRSVPGQMVALSSILSGILIMAFPATSIFHTFSHSYLELKKEQEQLQARLRHLQNTGPASECELLDPHVASEHELMNDVNDLILEGPALPIMHM

PDB Structures

Ligand Binding

1. DICL_CP

2. DICL_Pep

Binding Site

Disease

Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2G and Brown-Vialetto-Van Laere Syndrome 1

Location

Highly expressed in brain; and at lower levels in liver; small intestine and colon.

DOI ID

10.1073/pnas.122617999; 10.1101/gr.2596504; 10.1074/jbc.m808786200

RefSeq

NP_758857.1 [Q8TDN1-1]

Feature