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

Protein ID

ICDB_Pro_0409

Protein Name

Potassium voltage-gated channel subfamily A member 4

Gene Name

KCNA4; KCNA4L

Organism

Homo sapiens (Human)

Length

653 amino acids

AlphaFoldDB

AF-P22459-F1-model_v4.pdb

Function

Voltage-gated potassium channel that mediates transmembrane potassium transport in excitable membranes. Forms tetrameric potassium-selective channels through which potassium ions pass in accordance with their electrochemical gradient. The channel alternates between opened and closed conformations in response to the voltage difference across the membrane. Can form functional homotetrameric channels and heterotetrameric channels that contain variable proportions of KCNA1;KCNA2;KCNA4;KCNA5;and possibly other family members as well; channel properties depend on the type of alpha subunits that are part of the channel. Channel properties are modulated by cytoplasmic beta subunits that regulate the subcellular location of the alpha subunits and promote rapid inactivation. In vivo;membranes probably contain a mixture of heteromeric potassium channel complexes;making it difficult to assign currents observed in intact tissues to any particular potassium channel family member. Homotetrameric KCNA4 forms a potassium channel that opens in response to membrane depolarization;followed by rapid spontaneous channel closure. Likewise;a heterotetrameric channel formed by KCNA1 and KCNA4 shows rapid inactivation

Sequence

MEVAMVSAESSGCNSHMPYGYAAQARARERERLAHSRAAAAAAVAAATAAVEGSGGSGGGSHHHHQSRGACTSHDPQSSRGSRRRRRQRSEKKKAHYRQSSFPHCSDLMPSGSEEKILRELSEEEEDEEEEEEEEEEGRFYYSEDDHGDECSYTDLLPQDEGGGGYSSVRYSDCCERVVINVSGLRFETQMKTLAQFPETLLGDPEKRTQYFDPLRNEYFFDRNRPSFDAILYYYQSGGRLKRPVNVPFDIFTEEVKFYQLGEEALLKFREDEGFVREEEDRALPENEFKKQIWLLFEYPESSSPARGIAIVSVLVILISIVIFCLETLPEFRDDRDLVMALSAGGHGGLLNDTSAPHLENSGHTIFNDPFFIVETVCIVWFSFEFVVRCFACPSQALFFKNIMNIIDIVSILPYFITLGTDLAQQQGGGNGQQQQAMSFAILRIIRLVRVFRIFKLSRHSKGLQILGHTLRASMRELGLLIFFLFIGVILFSSAVYFAEADEPTTHFQSIPDAFWWAVVTMTTVGYGDMKPITVGGKIVGSLCAIAGVLTIALPVPVIVSNFNYFYHRETENEEQTQLTQNAVSCPYLPSNLLKKFRSSTSSSLGDKSEYLEMEEGVKESLCAKEEKCQGKGDDSETDKNNCSNAKAVETDV

PDB Structures

Ligand Binding

1. DICL_CP

2. DICL_Pep

Binding Site

Disease

Microcephaly;Cataracts;Impaired Intellectual Development;And Dystonia With Abnormal Striatum and Episodic Ataxia;Type 2

Location

Expressed in brain; and at lower levels in the testis; lung; kidney; colon and heart. Detected in heart ventricle.

DOI ID

10.1093/nar/18.23.7160; 10.1096/fasebj.5.3.2001794; 10.1016/1044-7431(90)90004-n; 10.1038/nature04632; 10.1161/01.res.72.6.1326; 10.1111/j.1460-9568.2006.05186.x; 10.1016/j.bbrc.2009.11.143; 10.1136/jmedgenet-2015-103637; 10.1038/385272a0

RefSeq

NP_002224.1

Feature