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Q96KK3 (KCNS1_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 98. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Potassium voltage-gated channel subfamily S member 1
Alternative name(s):
Delayed-rectifier K(+) channel alpha subunit 1
Voltage-gated potassium channel subunit Kv9.1
Gene names
Name:KCNS1
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length526 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Potassium channel subunit. Modulates channel activity and reduces the ion flow By similarity.

Subunit structure

Heteromultimer with KCNB1 and with KCNB2. Does not form homomultimers. Might also bind to other channel proteins By similarity.

Subcellular location

Cell membrane; Multi-pass membrane protein. Note: May not reach the plasma membrane but remain in an intracellular compartment in the absence of KCNB1.

Tissue specificity

Detected in all tissues tested with the exception of skeletal muscle. Highly expressed in adult and fetal brain, fetal kidney and lung, and adult prostate and testis.

Domain

The segment S4 is probably the voltage-sensor and is characterized by a series of positively charged amino acids at every third position.

Sequence similarities

Belongs to the potassium channel family. S (TC 1.A.1.2) subfamily. Kv9.1/KCNS1 sub-subfamily. [View classification]

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 526526Potassium voltage-gated channel subfamily S member 1
PRO_0000054081

Regions

Topological domain1 – 221221Cytoplasmic Potential
Transmembrane222 – 24221Helical; Name=Segment S1; Potential
Transmembrane275 – 29521Helical; Name=Segment S2; Potential
Topological domain296 – 30611Cytoplasmic Potential
Transmembrane307 – 32721Helical; Name=Segment S3; Potential
Transmembrane340 – 36021Helical; Voltage-sensor; Name=Segment S4; Potential
Topological domain361 – 37515Cytoplasmic Potential
Transmembrane376 – 39621Helical; Name=Segment S5; Potential
Intramembrane409 – 42921Pore-forming; Name=Segment H5; Potential
Transmembrane437 – 45721Helical; Name=Segment S6; Potential
Topological domain458 – 52669Cytoplasmic Potential
Motif421 – 4266Selectivity filter By similarity
Compositional bias250 – 25910Poly-Ala

Natural variations

Natural variant4891I → V. Ref.3
Corresponds to variant rs734784 [ dbSNP | Ensembl ].
VAR_020052
Natural variant5081Q → R.
Corresponds to variant rs7264544 [ dbSNP | Ensembl ].
VAR_053867

Sequences

Sequence LengthMass (Da)Tools
Q96KK3 [UniParc].

Last modified March 1, 2002. Version 2.
Checksum: 00F0E415E3A68C91

FASTA52658,372
        10         20         30         40         50         60 
MLMLLVRGTH YENLRSKVVL PTPLGGRSTE TFVSEFPGPD TGIRWRRSDE ALRVNVGGVR 

        70         80         90        100        110        120 
RQLSARALAR FPGTRLGRLQ AAASEEQARR LCDDYDEAAR EFYFDRHPGF FLSLLHFYRT 

       130        140        150        160        170        180 
GHLHVLDELC VFAFGQEADY WGLGENALAA CCRARYLERR LTQPHAWDED SDTPSSVDPC 

       190        200        210        220        230        240 
PDEISDVQRE LARYGAARCG RLRRRLWLTM ENPGYSLPSK LFSCVSISVV LASIAAMCIH 

       250        260        270        280        290        300 
SLPEYQAREA AAAVAAVAAG RSPEGVRDDP VLRRLEYFCI AWFSFEVSSR LLLAPSTRNF 

       310        320        330        340        350        360 
FCHPLNLIDI VSVLPFYLTL LAGVALGDQG GKEFGHLGKV VQVFRLMRIF RVLKLARHST 

       370        380        390        400        410        420 
GLRSLGATLK HSYREVGILL LYLAVGVSVF SGVAYTAEKE EDVGFNTIPA CWWWGTVSMT 

       430        440        450        460        470        480 
TVGYGDVVPV TVAGKLAASG CILGGILVVA LPITIIFNKF SHFYRRQKAL EAAVRNSNHQ 

       490        500        510        520 
EFEDLLSSID GVSEASLETS RETSQEGQSA DLESQAPSEP PHPQMY 

« Hide

References

« Hide 'large scale' references
[1]"Electrically silent potassium channel subunits from human lens epithelium."
Shepard A.R., Rae J.L.
Am. J. Physiol. 277:C412-C424(1999) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
Tissue: Brain and Lens epithelium.
[2]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"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 VAL-489.
Tissue: Brain.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF043473 mRNA. Translation: AAC13165.2.
Z93016 Genomic DNA. Translation: CAB07507.2.
BC075033 mRNA. Translation: AAH75033.2.
BC075034 mRNA. Translation: AAH75034.2.
BC132959 mRNA. Translation: AAI32960.1.
BC144234 mRNA. Translation: AAI44235.1.
IPIIPI00102065.
RefSeqNP_002242.2. NM_002251.3.
UniGeneHs.117780.

3D structure databases

ProteinModelPortalQ96KK3.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000307694.

Protein family/group databases

TCDB1.A.1.2.7. voltage-gated ion channel (VIC) superfamily.

PTM databases

PhosphoSiteQ96KK3.

Polymorphism databases

DMDM24418474.

Proteomic databases

PaxDbQ96KK3.
PRIDEQ96KK3.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000306117; ENSP00000307694; ENSG00000124134.
ENST00000537075; ENSP00000445595; ENSG00000124134.
GeneID3787.
KEGGhsa:3787.
UCSCuc002xnc.3. human.

Organism-specific databases

CTD3787.
GeneCardsGC20M043720.
HGNCHGNC:6300. KCNS1.
MIM602905. gene.
neXtProtNX_Q96KK3.
PharmGKBPA30078.
GenAtlasSearch...

Phylogenomic databases

eggNOGCOG1226.
HOGENOMHOG000231016.
HOVERGENHBG052230.
InParanoidQ96KK3.
KOK04931.
OMAFSCVSIS.
OrthoDBEOG4NS3B8.

Enzyme and pathway databases

ReactomeREACT_13685. Neuronal System.

Gene expression databases

ArrayExpressQ96KK3.
BgeeQ96KK3.
CleanExHS_KCNS1.
GenevestigatorQ96KK3.
GermOnlineENSG00000124134. Homo sapiens.

Family and domain databases

Gene3D3.30.710.10. 1 hit.
InterProIPR000210. BTB/POZ-like.
IPR011333. BTB/POZ_fold.
IPR005821. Ion_trans_dom.
IPR003091. K_chnl.
IPR003968. K_chnl_volt-dep_Kv.
IPR003971. K_chnl_volt-dep_Kv9.
IPR003131. T1-type_BTB.
[Graphical view]
PANTHERPTHR11537. PTHR11537. 1 hit.
PfamPF00520. Ion_trans. 1 hit.
PF02214. K_tetra. 1 hit.
[Graphical view]
PRINTSPR00169. KCHANNEL.
PR01494. KV9CHANNEL.
PR01491. KVCHANNEL.
SMARTSM00225. BTB. 1 hit.
[Graphical view]
SUPFAMSSF54695. BTB/POZ_fold. 1 hit.
ProtoNetSearch...

Other

GenomeRNAi3787.
NextBio14875.
SOURCESearch...

Entry information

Entry nameKCNS1_HUMAN
AccessionPrimary (citable) accession number: Q96KK3
Secondary accession number(s): A2RUL9 expand/collapse secondary AC list , B7ZM31, O43652, Q6DJU6
Entry history
Integrated into UniProtKB/Swiss-Prot: October 25, 2002
Last sequence update: March 1, 2002
Last modified: May 1, 2013
This is version 98 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny 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 20

Human chromosome 20: 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