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A6NK97 (S22AK_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified April 3, 2013. Version 53. 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·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Solute carrier family 22 member 20
Alternative name(s):
Organic anion transporter 6
Gene names
Name:SLC22A20
Synonyms:OAT6
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length555 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Function

Organic anion transporter that mediates the uptake of estrone sulfate. Inhibited by probenecid, propionate, 2-methylbutyrate, 3-methylbutyrate, benzoate, heptanoate and 2-ethylhaxanoate. May act as an odorant transporter By similarity.

Subcellular location

Membrane; Multi-pass membrane protein Potential.

Sequence similarities

Belongs to the major facilitator (TC 2.A.1) superfamily. Organic cation transporter (TC 2.A.1.19) family. [View classification]

Sequence caution

The sequence BAD18487.1 differs from that shown. Reason: Erroneous initiation.

Ontologies

Keywords
   Biological processIon transport
Transport
   Cellular componentMembrane
   Coding sequence diversityAlternative splicing
Polymorphism
   DomainTransmembrane
Transmembrane helix
   PTMGlycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological_procession transport

Inferred from electronic annotation. Source: UniProtKB-KW

   Cellular_componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

   Molecular_functiontransmembrane transporter activity

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: A6NK97-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Note: No experimental confirmation available.
Isoform 2 (identifier: A6NK97-2)

The sequence of this isoform differs from the canonical sequence as follows:
     213-347: VEWMPTRGRT...RKVTCCLMVI → ASRVIPLAPP...KQILSSKFQS
     348-555: Missing.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 555555Solute carrier family 22 member 20
PRO_0000326428

Regions

Topological domain1 – 2323Cytoplasmic Potential
Transmembrane24 – 4421Helical; Potential
Topological domain45 – 13793Extracellular Potential
Transmembrane138 – 15821Helical; Potential
Topological domain159 – 1668Cytoplasmic Potential
Transmembrane167 – 18721Helical; Potential
Topological domain188 – 1947Extracellular Potential
Transmembrane195 – 21521Helical; Potential
Topological domain216 – 22510Cytoplasmic Potential
Transmembrane226 – 24621Helical; Potential
Topological domain247 – 2504Extracellular Potential
Transmembrane251 – 27121Helical; Potential
Topological domain272 – 33968Cytoplasmic Potential
Transmembrane340 – 36021Helical; Potential
Topological domain361 – 37313Extracellular Potential
Transmembrane374 – 39421Helical; Potential
Topological domain395 – 3973Cytoplasmic Potential
Transmembrane398 – 41821Helical; Potential
Topological domain419 – 42911Extracellular Potential
Transmembrane430 – 45021Helical; Potential
Topological domain451 – 48535Cytoplasmic Potential
Transmembrane486 – 50621Helical; Potential
Topological domain507 – 55549Extracellular Potential
Compositional bias23 – 264Poly-Leu

Amino acid modifications

Glycosylation541N-linked (GlcNAc...) Potential
Glycosylation1141N-linked (GlcNAc...) Potential

Natural variations

Alternative sequence213 – 347135VEWMP…CLMVI → ASRVIPLAPPAWQVPVSCTE SAEGGCNEREEGGRGKADQG GDELLHPKRVCKCLHLQLNL GPLPNPGHPQGHMLSHGDLR GRQRSSGSGEQGGSCEPESR NGRLPAVAPAGLGLPFVHLP LSAREKQILSSKFQS in isoform 2.
VSP_032653
Alternative sequence348 – 555208Missing in isoform 2.
VSP_032654
Natural variant581A → D.
Corresponds to variant rs11605576 [ dbSNP | Ensembl ].
VAR_040065
Natural variant1391A → V.
Corresponds to variant rs12420456 [ dbSNP | Ensembl ].
VAR_040066
Isoform 2:
Natural variant2441G → G.
Corresponds to variant rs514076 [ dbSNP | Ensembl ].

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified July 24, 2007. Version 1.
Checksum: 3F3D75A7FFB5E91C

FASTA55560,459
        10         20         30         40         50         60 
MAFTDLLDAL GSMGRFQLNH TALLLLPCGL LACHNFLQNF TAAVPPHHCR GPANHTEAST 

        70         80         90        100        110        120 
NDSGAWLRAT IPLDQLGAPE PCRRFTKPQW ALLSPNSSIP GAATEGCKDG WVYNRSVFPS 

       130        140        150        160        170        180 
TIVMEWDLVC EARTLRDLAQ SVYMAGVLVG AAVFGSLADR LGCKGPLVWS YLQLAASGAA 

       190        200        210        220        230        240 
TAYFSSFSAY CVFRFLMGMT FSGIILNSVS LVVEWMPTRG RTVAGILLGY SFTLGQLILA 

       250        260        270        280        290        300 
GVAYLIRPWR CLQFAISAPF LIFFLYSWWL PESSRWLLLH GKSQLAVQNL QKVAAMNGRK 

       310        320        330        340        350        360 
EEGERLTKEV MSSYIQSEFA SVCTSNSILD LFRTPAIRKV TCCLMVIWFS NSVAYYGLAM 

       370        380        390        400        410        420 
DLQKFGLSLY LVQALFGIIN TPAMLVATAT MIYVGRRATV ASFLILAGLM VIANMFVPEG 

       430        440        450        460        470        480 
TQILCTAQAA LGKGCLASSF ICVYLFTGEL YPTEIRQMGM GFASVHARLG GLTAPLVTTL 

       490        500        510        520        530        540 
GEYSTILPPV SFGATAILAG LAVCVLTETR NMPLVETIAA MERRVKEGSS KKHVEEKSEE 

       550 
ISLQQLRASP LKETI 

« Hide

Isoform 2 [UniParc].

Checksum: D03C6E98DCA8A298
Show »

FASTA34737,029

References

[1]"Complete sequencing and characterization of 21,243 full-length human cDNAs."
Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. expand/collapse author list , Yamamoto J., Saito K., Kawai Y., Isono Y., Nakamura Y., Nagahari K., Murakami K., Yasuda T., Iwayanagi T., Wagatsuma M., Shiratori A., Sudo H., Hosoiri T., Kaku Y., Kodaira H., Kondo H., Sugawara M., Takahashi M., Kanda K., Yokoi T., Furuya T., Kikkawa E., Omura Y., Abe K., Kamihara K., Katsuta N., Sato K., Tanikawa M., Yamazaki M., Ninomiya K., Ishibashi T., Yamashita H., Murakawa K., Fujimori K., Tanai H., Kimata M., Watanabe M., Hiraoka S., Chiba Y., Ishida S., Ono Y., Takiguchi S., Watanabe S., Yosida M., Hotuta T., Kusano J., Kanehori K., Takahashi-Fujii A., Hara H., Tanase T.-O., Nomura Y., Togiya S., Komai F., Hara R., Takeuchi K., Arita M., Imose N., Musashino K., Yuuki H., Oshima A., Sasaki N., Aotsuka S., Yoshikawa Y., Matsunawa H., Ichihara T., Shiohata N., Sano S., Moriya S., Momiyama H., Satoh N., Takami S., Terashima Y., Suzuki O., Nakagawa S., Senoh A., Mizoguchi H., Goto Y., Shimizu F., Wakebe H., Hishigaki H., Watanabe T., Sugiyama A., Takemoto M., Kawakami B., Yamazaki M., Watanabe K., Kumagai A., Itakura S., Fukuzumi Y., Fujimori Y., Komiyama M., Tashiro H., Tanigami A., Fujiwara T., Ono T., Yamada K., Fujii Y., Ozaki K., Hirao M., Ohmori Y., Kawabata A., Hikiji T., Kobatake N., Inagaki H., Ikema Y., Okamoto S., Okitani R., Kawakami T., Noguchi S., Itoh T., Shigeta K., Senba T., Matsumura K., Nakajima Y., Mizuno T., Morinaga M., Sasaki M., Togashi T., Oyama M., Hata H., Watanabe M., Komatsu T., Mizushima-Sugano J., Satoh T., Shirai Y., Takahashi Y., Nakagawa K., Okumura K., Nagase T., Nomura N., Kikuchi H., Masuho Y., Yamashita R., Nakai K., Yada T., Nakamura Y., Ohara O., Isogai T., Sugano S.
Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
Tissue: Synovium.
[2]"Human chromosome 11 DNA sequence and analysis including novel gene identification."
Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. expand/collapse author list , Jaffe D.B., LaButti K., Nicol R., Park H.-S., Seaman C., Sougnez C., Yang X., Zimmer A.R., Zody M.C., Birren B.W., Nusbaum C., Fujiyama A., Hattori M., Rogers J., Lander E.S., Sakaki Y.
Nature 440:497-500(2006) [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] (ISOFORM 2).

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AK131327 mRNA. Translation: BAD18487.1. Different initiation.
AP003068 Genomic DNA. No translation available.
BC146850 mRNA. Translation: AAI46851.1.
IPIIPI00418585.
IPI00783068.
RefSeqNP_001004326.4. NM_001004326.4.
UniGeneHs.532372.

3D structure databases

ProteinModelPortalA6NK97.
ModBaseSearch...

PTM databases

PhosphoSiteA6NK97.

Proteomic databases

PaxDbA6NK97.
PRIDEA6NK97.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

GeneID440044.
KEGGhsa:440044.
UCSCuc021qlg.1. human.
uc021qlh.1. human.

Organism-specific databases

CTD440044.
GeneCardsGC11P064981.
HGNCHGNC:29867. SLC22A20.
MIM611696. gene.
neXtProtNX_A6NK97.
PharmGKBPA162403493.
GenAtlasSearch...

Phylogenomic databases

eggNOGCOG0477.
HOGENOMHOG000234569.
HOVERGENHBG108433.
KOK08216.
OrthoDBEOG418BPG.

Gene expression databases

CleanExHS_SLC22A20.
GenevestigatorA6NK97.

Family and domain databases

InterProIPR020846. MFS_dom.
IPR016196. MFS_dom_general_subst_transpt.
IPR005828. Sub_transporter.
[Graphical view]
PfamPF00083. Sugar_tr. 1 hit.
[Graphical view]
SUPFAMSSF103473. MFS_gen_substrate_transporter. 1 hit.
PROSITEPS50850. MFS. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi440044.
NextBio108866.
SOURCESearch...

Entry information

Entry nameS22AK_HUMAN
AccessionPrimary (citable) accession number: A6NK97
Secondary accession number(s): B9EJB2, Q6ZN88
Entry history
Integrated into UniProtKB/Swiss-Prot: March 18, 2008
Last sequence update: July 24, 2007
Last modified: April 3, 2013
This is version 53 of the entry and version 1 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 11

Human chromosome 11: 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