Protein Details: Potassium voltage-gated channel subfamily KQT member 5

Protein ID

ICDB_Pro_1582

Protein Name

Potassium voltage-gated channel subfamily KQT member 5

Gene Name

KCNQ5

Organism

Homo sapiens (Human)

Length

932 amino acids

AlphaFoldDB

AF-Q9NR82-F1-model_v4.pdb

Function

Associates with KCNQ3 to form a potassium channel which contributes to M-type current;a slowly activating and deactivating potassium conductance which plays a critical role in determining the subthreshold electrical excitability of neurons. Therefore;it is important in the regulation of neuronal excitability. May contribute;with other potassium channels;to the molecular diversity of a heterogeneous population of M-channels;varying in kinetic and pharmacological properties;which underlie this physiologically important current. Insensitive to tetraethylammonium;but inhibited by barium;linopirdine and XE991. Activated by niflumic acid and the anticonvulsant retigabine. As the native M-channel;the potassium channel composed of KCNQ3 and KCNQ5 is also suppressed by activation of the muscarinic acetylcholine receptor CHRM1

Sequence

MPRHHAGGEEGGAAGLWVKSGAAAAAAGGGRLGSGMKDVESGRGRVLLNSAAARGDGLLLLGTRAATLGGGGGGLRESRRGKQGARMSLLGKPLSYTSSQSCRRNVKYRRVQNYLYNVLERPRGWAFIYHAFVFLLVFGCLILSVFSTIPEHTKLASSCLLILEFVMIVVFGLEFIIRIWSAGCCCRYRGWQGRLRFARKPFCVIDTIVLIASIAVVSAKTQGNIFATSALRSLRFLQILRMVRMDRRGGTWKLLGSVVYAHSKELITAWYIGFLVLIFSSFLVYLVEKDANKEFSTYADALWWGTITLTTIGYGDKTPLTWLGRLLSAGFALLGISFFALPAGILGSGFALKVQEQHRQKHFEKRRNPAANLIQCVWRSYAADEKSVSIATWKPHLKALHTCSPTKKEQGEASSSQKLSFKERVRMASPRGQSIKSRQASVGDRRSPSTDITAEGSPTKVQKSWSFNDRTRFRPSLRLKSSQPKPVIDADTALGTDDVYDEKGCQCDVSVEDLTPPLKTVIRAIRIMKFHVAKRKFKETLRPYDVKDVIEQYSAGHLDMLCRIKSLQTRVDQILGKGQITSDKKSREKITAEHETTDDLSMLGRVVKVEKQVQSIESKLDCLLDIYQQVLRKGSASALALASFQIPPFECEQTSDYQSPVDSKDLSGSAQNSGCLSRSTSANISRGLQFILTPNEFSAQTFYALSPTMHSQATQVPISQSDGSAVAATNTIANQINTAPKPAAPTTLQIPPPLPAIKHLPRPETLHPNPAGLQESISDVTTCLVASKENVQVAQSNLTKDRSMRKSFDMGGETLLSVCPMVPKDLGKSLSVQNLIRSTEELNIQLSGSESSGSRGSQDFYPKWRESKLFITDEEVGPEETETDTFDAAPQPAREAAFASDSLRTGRSRSSQSICKAGESTDALSLPHVKLK

PDB Structures

Ligand Binding

1. DICL_CP

2. DICL_Pep

Binding Site

Disease

Intellectual Developmental Disorder;Autosomal Dominant 46 and Autosomal Dominant Non-Syndromic Intellectual Disability

Location

subregions of the brain and in skeletal muscle

DOI ID

10.1074/jbc.m002378200; 10.1038/nature02055; 10.1101/gr.2596504; 10.1038/ng1285; 10.1074/jbc.m003245200; 10.1038/sj.bjp.0703861; 10.1021/pr300630k; 10.1161/atvbaha.114.303801; 10.1016/j.neuron.2018.01.035; 10.1126/science.1133427; 10.1016/j.ajhg.2017.05.016

RefSeq

NP_001153602.1 [Q9NR82-2]; NP_001153604.1 [Q9NR82-3]; NP_001153605.1 [Q9NR82-6]; NP_001153606.1 [Q9NR82-5]; NP_062816.2 [Q9NR82-1]

Feature