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SO1A3_RAT
ID   SO1A3_RAT               Reviewed;         670 AA.
AC   P70502; Q8R008; Q8R4J0; Q8R4J1; Q8R4J2; Q8R4J3; Q8R4J4; Q8R4J5; Q8R4J6;
AC   Q8R4J7; Q8R4J8; Q8R4J9; Q8R4K0; Q8R4K1; Q9WTM0;
DT   30-MAY-2000, integrated into UniProtKB/Swiss-Prot.
DT   10-JAN-2003, sequence version 2.
DT   03-AUG-2022, entry version 153.
DE   RecName: Full=Solute carrier organic anion transporter family member 1A3;
DE   AltName: Full=OAT-K2;
DE   AltName: Full=Sodium-independent organic anion transporter K1;
DE            Short=OAT-K1;
DE   AltName: Full=Solute carrier family 21 member 4;
DE   AltName: Full=rOAT-K;
GN   Name=Slco1a3; Synonyms=Oatp1a3, Slc21a4;
OS   Rattus norvegicus (Rat).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae;
OC   Murinae; Rattus.
OX   NCBI_TaxID=10116;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1).
RC   STRAIN=Sprague-Dawley; TISSUE=Kidney;
RX   PubMed=8702823; DOI=10.1074/jbc.271.34.20719;
RA   Saito H., Masuda S., Inui K.;
RT   "Cloning and functional characterization of a novel rat organic anion
RT   transporter mediating basolateral uptake of methotrexate in the kidney.";
RL   J. Biol. Chem. 271:20719-20725(1996).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 13).
RC   TISSUE=Kidney;
RX   PubMed=10101033;
RA   Masuda S., Ibaramoto K., Takeuchi A., Saito H., Hashimoto Y., Inui K.;
RT   "Cloning and functional characterization of a new multispecific organic
RT   anion transporter, OAT-K2, in rat kidney.";
RL   Mol. Pharmacol. 55:743-752(1999).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 2; 3; 4; 5; 6; 7; 8; 9; 10; 11; 12; 14
RP   AND 15).
RC   STRAIN=Sprague-Dawley; TISSUE=Kidney;
RX   PubMed=12180133; DOI=10.1080/10425170290019856;
RA   Wolff M.W., Su T.-Z.;
RT   "Cloning and tissue-specific expression of spliced variants of the rat
RT   organic anion transporter (rOAT-K).";
RL   DNA Seq. 13:15-25(2002).
CC   -!- FUNCTION: Mediates the Na(+)-independent transport of organic anions
CC       such as methotrexate, taurocholate, folate and prostaglandin E2. May
CC       contribute to renal secretion and/or reabsorption of hydrophobic
CC       anionic compounds. Mediates renal clearance of methotrexate from the
CC       blood.
CC   -!- SUBCELLULAR LOCATION: Cell membrane; Multi-pass membrane protein.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=15;
CC       Name=1;
CC         IsoId=P70502-1; Sequence=Displayed;
CC       Name=2; Synonyms=K1;
CC         IsoId=P70502-2; Sequence=VSP_006143, VSP_006145;
CC       Name=3; Synonyms=K5;
CC         IsoId=P70502-3; Sequence=VSP_006133, VSP_006143, VSP_006145;
CC       Name=4; Synonyms=K6;
CC         IsoId=P70502-4; Sequence=VSP_006143, VSP_006144;
CC       Name=5; Synonyms=K14;
CC         IsoId=P70502-5; Sequence=VSP_006134, VSP_006140, VSP_006143,
CC                                  VSP_006145;
CC       Name=6; Synonyms=K3;
CC         IsoId=P70502-6; Sequence=VSP_006133, VSP_006143, VSP_006144;
CC       Name=7; Synonyms=K8;
CC         IsoId=P70502-7; Sequence=VSP_006135, VSP_006141, VSP_006143,
CC                                  VSP_006145;
CC       Name=8; Synonyms=K2;
CC         IsoId=P70502-8; Sequence=VSP_006136, VSP_006143, VSP_006145;
CC       Name=9; Synonyms=K4, K13;
CC         IsoId=P70502-9; Sequence=VSP_006139, VSP_006146;
CC       Name=10; Synonyms=K12;
CC         IsoId=P70502-10; Sequence=VSP_006137, VSP_006143, VSP_006144;
CC       Name=11; Synonyms=K7;
CC         IsoId=P70502-11; Sequence=VSP_006136, VSP_006143, VSP_006144;
CC       Name=12; Synonyms=K11;
CC         IsoId=P70502-12; Sequence=VSP_006135, VSP_006141, VSP_006143,
CC                                   VSP_006144;
CC       Name=13; Synonyms=K2;
CC         IsoId=P70502-13; Sequence=VSP_006138, VSP_006142, VSP_006143,
CC                                   VSP_006145;
CC       Name=14; Synonyms=K9;
CC         IsoId=P70502-14; Sequence=VSP_006137, VSP_006143, VSP_006145;
CC       Name=15; Synonyms=K10;
CC         IsoId=P70502-15; Sequence=VSP_006134, VSP_006140, VSP_006143,
CC                                   VSP_006144;
CC   -!- TISSUE SPECIFICITY: All isoforms are detected in kidney, and many are
CC       kidney specific. Isoforms 2 and 13 are also detected in liver. Isoforms
CC       4 and 9/K4 are ubiquitous, but isoform 9/K13 is kidney specific.
CC       Isoforms 5 and 14 are detected in all tissues tested, with the
CC       exception of pancreas and spleen. Isoforms 11 and 15 are detected in
CC       kidney, pancreas and testis. Isoform 7 is detected in kidney, liver,
CC       testis and spleen.
CC   -!- SIMILARITY: Belongs to the organo anion transporter (TC 2.A.60) family.
CC       {ECO:0000305}.
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DR   EMBL; D79981; BAA11476.1; -; mRNA.
DR   EMBL; AB012662; BAA77793.1; -; mRNA.
DR   EMBL; AF445993; AAL84221.1; -; mRNA.
DR   EMBL; AF445994; AAL84222.1; -; mRNA.
DR   EMBL; AF445995; AAL84223.1; -; mRNA.
DR   EMBL; AF445996; AAL84224.1; -; mRNA.
DR   EMBL; AF445997; AAL84225.1; -; mRNA.
DR   EMBL; AF445998; AAL84226.1; -; mRNA.
DR   EMBL; AF445999; AAL84227.1; -; mRNA.
DR   EMBL; AF446000; AAL84228.1; -; mRNA.
DR   EMBL; AF446001; AAL84229.1; -; mRNA.
DR   EMBL; AF446002; AAL84230.1; -; mRNA.
DR   EMBL; AF446003; AAL84231.1; -; mRNA.
DR   EMBL; AF446004; AAL84232.1; -; mRNA.
DR   EMBL; AF446005; AAL84233.1; -; mRNA.
DR   EMBL; AF446006; AAL84234.1; -; mRNA.
DR   RefSeq; NP_110464.1; NM_030837.1. [P70502-2]
DR   AlphaFoldDB; P70502; -.
DR   SMR; P70502; -.
DR   STRING; 10116.ENSRNOP00000015112; -.
DR   BindingDB; P70502; -.
DR   ChEMBL; CHEMBL2073707; -.
DR   TCDB; 2.A.60.1.4; the organo anion transporter (oat) family.
DR   GlyGen; P70502; 4 sites.
DR   iPTMnet; P70502; -.
DR   PhosphoSitePlus; P70502; -.
DR   PaxDb; P70502; -.
DR   Ensembl; ENSRNOT00000000026; ENSRNOP00000000026; ENSRNOG00000010388. [P70502-2]
DR   GeneID; 80899; -.
DR   KEGG; rno:80899; -.
DR   CTD; 80899; -.
DR   RGD; 621387; Slc21a4.
DR   VEuPathDB; HostDB:ENSRNOG00000030894; -.
DR   VEuPathDB; HostDB:ENSRNOG00000047493; -.
DR   eggNOG; KOG3626; Eukaryota.
DR   GeneTree; ENSGT01050000244856; -.
DR   HOGENOM; CLU_729505_0_0_1; -.
DR   InParanoid; P70502; -.
DR   OrthoDB; 1029129at2759; -.
DR   PhylomeDB; P70502; -.
DR   TreeFam; TF317540; -.
DR   PRO; PR:P70502; -.
DR   Proteomes; UP000002494; Chromosome 4.
DR   Bgee; ENSRNOG00000010388; Expressed in adult mammalian kidney and 8 other tissues.
DR   ExpressionAtlas; P70502; baseline and differential.
DR   Genevisible; P70502; RN.
DR   GO; GO:0005887; C:integral component of plasma membrane; IBA:GO_Central.
DR   GO; GO:0015125; F:bile acid transmembrane transporter activity; IBA:GO_Central.
DR   GO; GO:0008514; F:organic anion transmembrane transporter activity; IDA:RGD.
DR   GO; GO:0015347; F:sodium-independent organic anion transmembrane transporter activity; IBA:GO_Central.
DR   GO; GO:0098656; P:anion transmembrane transport; IDA:RGD.
DR   GO; GO:0015721; P:bile acid and bile salt transport; IBA:GO_Central.
DR   GO; GO:0043252; P:sodium-independent organic anion transport; IBA:GO_Central.
DR   Gene3D; 1.20.1250.20; -; 1.
DR   InterPro; IPR002350; Kazal_dom.
DR   InterPro; IPR036058; Kazal_dom_sf.
DR   InterPro; IPR036259; MFS_trans_sf.
DR   InterPro; IPR004156; OATP.
DR   PANTHER; PTHR11388; PTHR11388; 1.
DR   Pfam; PF07648; Kazal_2; 1.
DR   Pfam; PF03137; OATP; 1.
DR   SUPFAM; SSF100895; SSF100895; 1.
DR   SUPFAM; SSF103473; SSF103473; 1.
DR   TIGRFAMs; TIGR00805; oat; 1.
DR   PROSITE; PS51465; KAZAL_2; 1.
PE   2: Evidence at transcript level;
KW   Alternative splicing; Cell membrane; Disulfide bond; Glycoprotein;
KW   Ion transport; Membrane; Reference proteome; Transmembrane;
KW   Transmembrane helix; Transport.
FT   CHAIN           1..670
FT                   /note="Solute carrier organic anion transporter family
FT                   member 1A3"
FT                   /id="PRO_0000191045"
FT   TOPO_DOM        1..20
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        21..40
FT                   /note="Helical; Name=1"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        41..59
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        60..80
FT                   /note="Helical; Name=2"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        81..86
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        87..111
FT                   /note="Helical; Name=3"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        112..155
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        156..184
FT                   /note="Helical; Name=4"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        185..203
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        204..224
FT                   /note="Helical; Name=5"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        225..242
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        243..267
FT                   /note="Helical; Name=6"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        268..311
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        312..333
FT                   /note="Helical; Name=7"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        334..353
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        354..377
FT                   /note="Helical; Name=8"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        378..381
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        382..405
FT                   /note="Helical; Name=9"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        406..513
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        514..536
FT                   /note="Helical; Name=10"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        537..545
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        546..571
FT                   /note="Helical; Name=11"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        572..605
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        606..623
FT                   /note="Helical; Name=12"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        624..670
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   DOMAIN          433..488
FT                   /note="Kazal-like"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00798"
FT   REGION          277..296
FT                   /note="Disordered"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   COMPBIAS        279..296
FT                   /note="Basic and acidic residues"
FT                   /evidence="ECO:0000256|SAM:MobiDB-lite"
FT   CARBOHYD        124
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        135
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        483
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        492
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   DISULFID        439..469
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00798"
FT   DISULFID        445..465
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00798"
FT   DISULFID        454..486
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00798"
FT   VAR_SEQ         1..318
FT                   /note="Missing (in isoform 9)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006139"
FT   VAR_SEQ         1..172
FT                   /note="Missing (in isoform 13)"
FT                   /evidence="ECO:0000303|PubMed:10101033"
FT                   /id="VSP_006138"
FT   VAR_SEQ         1..156
FT                   /note="Missing (in isoform 10 and isoform 14)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006137"
FT   VAR_SEQ         1..132
FT                   /note="Missing (in isoform 8 and isoform 11)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006136"
FT   VAR_SEQ         1..102
FT                   /note="Missing (in isoform 7 and isoform 12)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006135"
FT   VAR_SEQ         1..61
FT                   /note="Missing (in isoform 5 and isoform 15)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006134"
FT   VAR_SEQ         1..23
FT                   /note="Missing (in isoform 3 and isoform 6)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006133"
FT   VAR_SEQ         62..67
FT                   /note="NGSFEI -> MLCQDQ (in isoform 5 and isoform 15)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006140"
FT   VAR_SEQ         103..111
FT                   /note="ISLPHFLMG -> MGPDALPRS (in isoform 7 and isoform
FT                   12)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006141"
FT   VAR_SEQ         173
FT                   /note="T -> M (in isoform 13)"
FT                   /evidence="ECO:0000303|PubMed:10101033"
FT                   /id="VSP_006142"
FT   VAR_SEQ         289..298
FT                   /note="STEKRPRKKN -> KHREKAKEEK (in isoform 2, isoform 3,
FT                   isoform 4, isoform 5, isoform 6, isoform 7, isoform 8,
FT                   isoform 10, isoform 11, isoform 12, isoform 13, isoform 14
FT                   and isoform 15)"
FT                   /evidence="ECO:0000303|PubMed:10101033,
FT                   ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006143"
FT   VAR_SEQ         304..358
FT                   /note="Missing (in isoform 4, isoform 6, isoform 10,
FT                   isoform 11, isoform 12 and isoform 15)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006144"
FT   VAR_SEQ         312..325
FT                   /note="PVLQPDLHAVHPYK -> LSCNPIYMLFTLIS (in isoform 2,
FT                   isoform 3, isoform 5, isoform 7, isoform 8, isoform 13 and
FT                   isoform 14)"
FT                   /evidence="ECO:0000303|PubMed:10101033,
FT                   ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006145"
FT   VAR_SEQ         319..325
FT                   /note="HAVHPYK -> MLFTLIS (in isoform 9)"
FT                   /evidence="ECO:0000303|PubMed:12180133"
FT                   /id="VSP_006146"
FT   CONFLICT        391
FT                   /note="A -> R (in Ref. 1; BAA11476)"
FT                   /evidence="ECO:0000305"
FT   CONFLICT        588..589
FT                   /note="AC -> R (in Ref. 1; BAA11476)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   670 AA;  73817 MW;  E05F0B34A4C0ED9F CRC64;
     MGDLEKGAAT HGAGCFAKIK VFLMALTCAY VSKSLSGTFM SSMLTQIERQ FGIPTAIVGF
     INGSFEIGNL LLIIFVSYFG MKLHRPIVIG VGCAVMGLGC FIISLPHFLM GRYEYETTIL
     PTSNLSSNSF LCMENQTQTL NPAQDPAECV KEVKSLMWIY VLVGNIIRGI GETPIMPLGV
     SYIENFAKSE NSPLYIGILE TGKMIGPIFG LLLGSFCASI YVDTGSVNTD DLTITPTDIR
     WVGAWWIGFL VCAGVNILIS IPFFFFPKTL PKEGLQENVD GTENAKEEST EKRPRKKNRG
     ITKDFFPFLK SPVLQPDLHA VHPYKVLQVN AFNIYFSFLP KYLENQYGKS TAEVIFLMGV
     YNLPAICIGY LIAGFMMKKF KITVKTAAFL AFCLSLSEYS FGFCNFLITC DNVPVAGLTN
     SYERDQKPLY LENNVLADCN TRCSCLTKTW DPVCGDNGLA YMSACLAGCE KSVGTGTNMV
     FHNCSCIQSP GNSSAVLGLC NKGPECTNKL QYLLILSGFL SILYSFAAIP GYMVFLRCIK
     SEEKSLGIGI HAFCIRVFAG IPAPIYFGAL IDRTCLHWGT QKCGAPGACR MYDINSFRRI
     YLGMSAALRG SSYLPAFVIV ILTRKFSLPG KINSSEMEIA EMKLTEKESQ CTDVHRNPKF
     KNDGELKTKL
 
 
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