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RHBG_BOVIN
ID   RHBG_BOVIN              Reviewed;         455 AA.
AC   Q95M77; A3KMW3;
DT   03-APR-2007, integrated into UniProtKB/Swiss-Prot.
DT   10-FEB-2009, sequence version 2.
DT   03-AUG-2022, entry version 105.
DE   RecName: Full=Ammonium transporter Rh type B;
DE   AltName: Full=Rhesus blood group family type B glycoprotein;
DE            Short=Rh family type B glycoprotein;
DE            Short=Rh type B glycoprotein;
GN   Name=RHBG;
OS   Bos taurus (Bovine).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Bovidae;
OC   Bovinae; Bos.
OX   NCBI_TaxID=9913;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2).
RX   PubMed=11358367; DOI=10.1006/bcmd.2000.0355;
RA   Huang C.-H., Liu P.Z.;
RT   "New insights into the Rh superfamily of genes and proteins in erythroid
RT   cells and nonerythroid tissues.";
RL   Blood Cells Mol. Dis. 27:90-101(2001).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
RC   STRAIN=Hereford; TISSUE=Fetal skin;
RG   NIH - Mammalian Gene Collection (MGC) project;
RL   Submitted (FEB-2007) to the EMBL/GenBank/DDBJ databases.
CC   -!- FUNCTION: Functions as a specific ammonium transporter. {ECO:0000250}.
CC   -!- SUBUNIT: Interacts (via C-terminus) with ANK2 and ANK3; required for
CC       targeting to the basolateral membrane. {ECO:0000250}.
CC   -!- SUBCELLULAR LOCATION: Basolateral cell membrane {ECO:0000250}; Multi-
CC       pass membrane protein {ECO:0000250}. Cytoplasmic vesicle membrane
CC       {ECO:0000250}; Multi-pass membrane protein {ECO:0000250}.
CC   -!- ALTERNATIVE PRODUCTS:
CC       Event=Alternative splicing; Named isoforms=2;
CC       Name=1;
CC         IsoId=Q95M77-1; Sequence=Displayed;
CC       Name=2;
CC         IsoId=Q95M77-2; Sequence=VSP_036401, VSP_036402;
CC   -!- PTM: N-glycosylated. {ECO:0000250}.
CC   -!- SIMILARITY: Belongs to the ammonium transporter (TC 2.A.49) family. Rh
CC       subfamily. {ECO:0000305}.
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DR   EMBL; AY013259; AAK14649.1; -; mRNA.
DR   EMBL; BC133318; AAI33319.1; -; mRNA.
DR   RefSeq; NP_777148.1; NM_174723.2.
DR   RefSeq; XP_005203673.1; XM_005203616.3. [Q95M77-1]
DR   AlphaFoldDB; Q95M77; -.
DR   SMR; Q95M77; -.
DR   STRING; 9913.ENSBTAP00000046932; -.
DR   PaxDb; Q95M77; -.
DR   Ensembl; ENSBTAT00000050191; ENSBTAP00000046932; ENSBTAG00000012234. [Q95M77-1]
DR   GeneID; 282709; -.
DR   KEGG; bta:282709; -.
DR   CTD; 57127; -.
DR   VEuPathDB; HostDB:ENSBTAG00000012234; -.
DR   eggNOG; KOG3796; Eukaryota.
DR   GeneTree; ENSGT00950000182844; -.
DR   HOGENOM; CLU_021386_0_0_1; -.
DR   InParanoid; Q95M77; -.
DR   OMA; IFVRYNH; -.
DR   OrthoDB; 910733at2759; -.
DR   TreeFam; TF314450; -.
DR   Reactome; R-BTA-444411; Rhesus glycoproteins mediate ammonium transport.
DR   Proteomes; UP000009136; Chromosome 3.
DR   Bgee; ENSBTAG00000012234; Expressed in urethra and 85 other tissues.
DR   ExpressionAtlas; Q95M77; baseline and differential.
DR   GO; GO:0046658; C:anchored component of plasma membrane; IEA:Ensembl.
DR   GO; GO:0016323; C:basolateral plasma membrane; ISS:UniProtKB.
DR   GO; GO:0030659; C:cytoplasmic vesicle membrane; IEA:UniProtKB-SubCell.
DR   GO; GO:0005887; C:integral component of plasma membrane; IBA:GO_Central.
DR   GO; GO:0014731; C:spectrin-associated cytoskeleton; ISS:UniProtKB.
DR   GO; GO:0008519; F:ammonium transmembrane transporter activity; ISS:UniProtKB.
DR   GO; GO:0030506; F:ankyrin binding; IEA:Ensembl.
DR   GO; GO:0097272; P:ammonium homeostasis; IBA:GO_Central.
DR   GO; GO:0072488; P:ammonium transmembrane transport; ISS:UniProtKB.
DR   GO; GO:0070634; P:transepithelial ammonium transport; IEA:Ensembl.
DR   Gene3D; 1.10.3430.10; -; 1.
DR   InterPro; IPR029020; Ammonium/urea_transptr.
DR   InterPro; IPR024041; NH4_transpt_AmtB-like_dom.
DR   InterPro; IPR002229; RhesusRHD.
DR   Pfam; PF00909; Ammonium_transp; 1.
DR   PRINTS; PR00342; RHESUSRHD.
PE   2: Evidence at transcript level;
KW   Alternative splicing; Ammonia transport; Cell membrane;
KW   Cytoplasmic vesicle; Glycoprotein; Membrane; Reference proteome;
KW   Transmembrane; Transmembrane helix; Transport.
FT   CHAIN           1..455
FT                   /note="Ammonium transporter Rh type B"
FT                   /id="PRO_0000283594"
FT   TOPO_DOM        1..13
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        14..34
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        35..61
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        62..82
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        83..86
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        87..107
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        108..124
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        125..145
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        146..151
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        152..172
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        173..179
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        180..200
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        201..219
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        220..240
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        241..253
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        254..274
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        275..277
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        278..298
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        299
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        300..320
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        321..343
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        344..364
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        365..393
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        394..414
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        415..455
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   REGION          416..424
FT                   /note="Interaction with ANK3"
FT                   /evidence="ECO:0000250"
FT   MOTIF           429..432
FT                   /note="Basolateral sorting signal"
FT                   /evidence="ECO:0000250"
FT   CARBOHYD        49
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   VAR_SEQ         168
FT                   /note="F -> FVLLSLLEVVLFGLNEF (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:11358367"
FT                   /id="VSP_036401"
FT   VAR_SEQ         281..326
FT                   /note="Missing (in isoform 2)"
FT                   /evidence="ECO:0000303|PubMed:11358367"
FT                   /id="VSP_036402"
FT   CONFLICT        208..209
FT                   /note="Missing (in Ref. 2; AAI33319)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   455 AA;  49193 MW;  4BAB3BBE2D26E9EE CRC64;
     MAWSPRHSAG RRLQLPLLCL LLQGATAILF AVFVRYNRET DAALWHWGNH SNADNEFYFR
     YPSFQDVHAM IFVGFGFLMV FLQRYGFGSV GFTFLLAAFA LQWSTLIQGF FHSFRGGYIL
     VGMESMINAD FCAGAVLISF GAVLGKTGPV QLLLMALLEV VLFGLNEFVL LSLLEVKDAG
     GSMTIHTFGA YFGLILSRVL YRPQLEKSKH RQGSVYHSDL FAMIGTIFLW IFWPSFNSAP
     TALGDGQHRT ALNTYYSLTA STLSTFALSA LVGGDGRLDM VHVQNAALAG GVVVGTSAEM
     MLTPFGALAA GFLAGAISTL GYKFVTPILE SKLKVQDTCG VHNLHGMPGV LGALLGGLVA
     GLATREAYGD GLESVFPLIA EGQRSATSQA MHQLFGLFVT LTFASVGGGL GGLLLRLPIL
     DSPPDSQCYE DQIYWEVPGE HEHLAQGSEE TETQA
 
 
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