Q6PIU1 (KCNV1_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 86.
History...
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Potassium voltage-gated channel subfamily V member 1 Alternative name(s): Neuronal potassium channel alpha subunit HNKA Voltage-gated potassium channel subunit Kv8.1 | ||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||
| Taxonomic identifier | 9606 [NCBI] | ||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 500 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Potassium channel subunit that does not form functional channels by itself. Modulates KCNB1 and KCNB2 channel activity by shifting the threshold for inactivation to more negative values and by slowing the rate of inactivation. Can down-regulate the channel activity of KCNB1, KCNB2, KCNC4 and KCND1, possibly by trapping them in intracellular membranes. Ref.1 Ref.5 |
| Subunit structure | Heteromultimer with KCNB1 and KCNB2. Interacts with KCNC4 and KCND1. Ref.1 Ref.5 |
| Subcellular location | Cell membrane; Multi-pass membrane protein. Note: Has to be associated with another potassium channel subunit to get inserted in the plasma membrane. Remains intracellular in the absence of KCNB2. Ref.1 Ref.5 |
| Tissue specificity | Detected in brain. Ref.2 |
| Domain | The segment S4 is probably the voltage-sensor and is characterized by a series of positively charged amino acids at every third position By similarity. |
| Sequence similarities | Belongs to the potassium channel family. V (TC 1.A.1.2) subfamily. Kv8.1/KCNV1 sub-subfamily. [View classification] |
Ontologies
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 500 | 500 | Potassium voltage-gated channel subfamily V member 1 | PRO_0000308350 | |||||
Regions | |||||||||
| Topological domain | 1 – 210 | 210 | Cytoplasmic Potential | ||||||
| Transmembrane | 211 – 231 | 21 | Helical; Name=Segment S1; Potential | ||||||
| Topological domain | 232 – 238 | 7 | Extracellular Potential | ||||||
| Transmembrane | 239 – 259 | 21 | Helical; Name=Segment S2; Potential | ||||||
| Topological domain | 260 – 276 | 17 | Cytoplasmic Potential | ||||||
| Transmembrane | 277 – 297 | 21 | Helical; Name=Segment S3; Potential | ||||||
| Topological domain | 298 – 309 | 12 | Extracellular Potential | ||||||
| Transmembrane | 310 – 331 | 22 | Helical; Voltage-sensor; Name=Segment S4; Potential | ||||||
| Topological domain | 332 – 345 | 14 | Cytoplasmic Potential | ||||||
| Transmembrane | 346 – 366 | 21 | Helical; Name=Segment S5; Potential | ||||||
| Transmembrane | 407 – 427 | 21 | Helical; Name=Segment S6; Potential | ||||||
| Topological domain | 428 – 500 | 73 | Cytoplasmic Potential | ||||||
| Motif | 392 – 397 | 6 | Selectivity filter By similarity | ||||||
Natural variations | |||||||||
| Natural variant | 22 | 1 | D → G. Ref.4 Corresponds to variant rs17852611 [ dbSNP | Ensembl ]. | VAR_036804 | |||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Kv8.1, a new neuronal potassium channel subunit with specific inhibitory properties towards Shab and Shaw channels." Hugnot J.-P., Salinas M., Lesage F., Guillemare E., de Weille J., Heurteaux C., Mattei M.-G., Lazdunski M. EMBO J. 15:3322-3331(1996) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA], FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH KCNB1; KCNB2; KCNC4 AND KCND1. |
| [2] | "Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy." Sano A., Mikami M., Nakamura M., Ueno S., Tanabe H., Kaneko S. Epilepsia 43:26-31(2002) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA], TISSUE SPECIFICITY. |
| [3] | "Molecular cloning of human neuronal potassium channel alpha subunit (HNKA)." Xia J.-H., Zheng D., Tang X.-X., Yu K.-P., Tan S. Submitted (DEC-1999) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA]. Tissue: Kidney. |
| [4] | "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)." The MGC Project Team Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT GLY-22. Tissue: Brain. |
| [5] | "Modes of regulation of shab K+ channel activity by the Kv8.1 subunit." Salinas M., de Weille J., Guillemare E., Lazdunski M., Hugnot J.-P. J. Biol. Chem. 272:8774-8780(1997) [PubMed] [Europe PMC] [Abstract] Cited for: FUNCTION, SUBCELLULAR LOCATION, INTERACTION WITH KCNB1 AND KCNB2. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AB032013 Genomic DNA. Translation: BAA92316.1. AF167082 mRNA. Translation: AAD48031.2. BC028739 mRNA. Translation: AAH28739.1. |
| IPI | IPI00164159. |
| RefSeq | NP_055194.1. NM_014379.2. |
| UniGene | Hs.13285. |
3D structure databases | |
| HSSP | HSSP built from PDB template 2A79 based on UniProtKB P63142. |
| ProteinModelPortal | Q6PIU1. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000297404. |
Polymorphism databases | |
| DMDM | 160013825. |
Proteomic databases | |
| PaxDb | Q6PIU1. |
| PRIDE | Q6PIU1. |
Protocols and materials databases | |
| DNASU | 27012. |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000297404; ENSP00000297404; ENSG00000164794. ENST00000524391; ENSP00000435954; ENSG00000164794. |
| GeneID | 27012. |
| KEGG | hsa:27012. |
| UCSC | uc003ynr.4. human. |
Organism-specific databases | |
| CTD | 27012. |
| GeneCards | GC08M111048. |
| HGNC | HGNC:18861. KCNV1. |
| MIM | 608164. gene. |
| neXtProt | NX_Q6PIU1. |
| PharmGKB | PA38721. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | COG1226. |
| HOGENOM | HOG000231016. |
| HOVERGEN | HBG052230. |
| InParanoid | Q6PIU1. |
| KO | K04934. |
| OMA | DRCHFLR. |
| OrthoDB | EOG4BRWKP. |
| PhylomeDB | Q6PIU1. |
Enzyme and pathway databases | |
| Reactome | REACT_13685. Neuronal System. |
Gene expression databases | |
| ArrayExpress | Q6PIU1. |
| Bgee | Q6PIU1. |
| CleanEx | HS_KCNV1. |
| Genevestigator | Q6PIU1. |
Family and domain databases | |
| Gene3D | 3.30.710.10. 1 hit. |
| InterPro | IPR000210. BTB/POZ-like. IPR011333. BTB/POZ_fold. IPR005821. Ion_trans_dom. IPR003091. K_chnl. IPR003968. K_chnl_volt-dep_Kv. IPR003970. K_chnl_volt-dep_Kv8. IPR003131. T1-type_BTB. [Graphical view] |
| PANTHER | PTHR11537. PTHR11537. 1 hit. PTHR11537:SF38. PTHR11537:SF38. 1 hit. |
| Pfam | PF00520. Ion_trans. 1 hit. PF02214. K_tetra. 1 hit. [Graphical view] |
| PRINTS | PR00169. KCHANNEL. PR01493. KV8CHANNEL. PR01491. KVCHANNEL. |
| SMART | SM00225. BTB. 1 hit. [Graphical view] |
| SUPFAM | SSF54695. BTB/POZ_fold. 1 hit. |
| ProtoNet | Search... |
Other | |
| GenomeRNAi | 27012. |
| NextBio | 49524. |
| SOURCE | Search... |
Entry information
| Entry name | KCNV1_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q6PIU1 Secondary accession number(s): Q9UHJ4 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| Human chromosome 8 Human chromosome 8: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
