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RHCG_PONAB
ID   RHCG_PONAB              Reviewed;         472 AA.
AC   Q5NVA3;
DT   03-APR-2007, integrated into UniProtKB/Swiss-Prot.
DT   04-JAN-2005, sequence version 1.
DT   25-MAY-2022, entry version 57.
DE   RecName: Full=Ammonium transporter Rh type C;
DE   AltName: Full=Rhesus blood group family type C glycoprotein;
DE            Short=Rh family type C glycoprotein;
DE            Short=Rh type C glycoprotein;
GN   Name=RHCG;
OS   Pongo abelii (Sumatran orangutan) (Pongo pygmaeus abelii).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Pongo.
OX   NCBI_TaxID=9601;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Kidney;
RG   The German cDNA consortium;
RL   Submitted (DEC-2004) to the EMBL/GenBank/DDBJ databases.
CC   -!- FUNCTION: Functions as an electroneutral and bidirectional ammonium
CC       transporter. May regulate transepithelial ammonia secretion (By
CC       similarity). {ECO:0000250}.
CC   -!- SUBUNIT: Homotrimer.
CC   -!- SUBCELLULAR LOCATION: Apical cell membrane {ECO:0000250}; Multi-pass
CC       membrane protein {ECO:0000250}. Note=Also detected at the basolateral
CC       membrane and in subapical vesicles. {ECO:0000250}.
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; CR926482; CAI30274.1; -; Transcribed_RNA.
DR   AlphaFoldDB; Q5NVA3; -.
DR   SMR; Q5NVA3; -.
DR   STRING; 9601.ENSPPYP00000007674; -.
DR   eggNOG; KOG3796; Eukaryota.
DR   InParanoid; Q5NVA3; -.
DR   Proteomes; UP000001595; Unplaced.
DR   GO; GO:0016324; C:apical plasma membrane; ISS:UniProtKB.
DR   GO; GO:0016323; C:basolateral plasma membrane; ISS:UniProtKB.
DR   GO; GO:0031410; C:cytoplasmic vesicle; ISS:UniProtKB.
DR   GO; GO:0005887; C:integral component of plasma membrane; ISS:UniProtKB.
DR   GO; GO:0008519; F:ammonium transmembrane transporter activity; ISS:UniProtKB.
DR   GO; GO:0030506; F:ankyrin binding; ISS:UniProtKB.
DR   GO; GO:0072488; P:ammonium transmembrane transport; ISS:UniProtKB.
DR   GO; GO:0006873; P:cellular ion homeostasis; ISS:UniProtKB.
DR   GO; GO:0070634; P:transepithelial ammonium transport; ISS:UniProtKB.
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   3: Inferred from homology;
KW   Ammonia transport; Cell membrane; Glycoprotein; Membrane;
KW   Reference proteome; Transmembrane; Transmembrane helix; Transport.
FT   CHAIN           1..472
FT                   /note="Ammonium transporter Rh type C"
FT                   /id="PRO_0000283582"
FT   TOPO_DOM        1..9
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        10..30
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        31..51
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        52..72
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        73..76
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        77..97
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        98..114
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        115..135
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        136..139
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        140..160
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        161..168
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        169..191
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        192..209
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        210..230
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        231..241
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        242..262
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        263..294
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        295..315
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        316..336
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        337..357
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        358..388
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        389..409
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        410..450
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        451..471
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        472
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   CARBOHYD        435
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
SQ   SEQUENCE   472 AA;  52321 MW;  667E8388CF019963 CRC64;
     MAWNTNLRWR LPLTCLLLEV VMVILFGVFV RYDFDADAHW WSWRTEFYYR YPSFQDVHVM
     VFVGFGFLMT FLQRYGFSAV GFNFLLAAFG IQWALLMQGW FHFLQGRYIV VGVENLINAD
     FCVASVCVAF GAVLGKVSPI QLLIMTFFQV TLFAVNEFIL LNLLKVKDAG GSMTIHTFGA
     YFGLTVTRIL YRRNLEQSKE RQNSVYQSDL FAMIGTLFLW MYWPSFNSAI SYHGDSQHRA
     AINTYCSLAA CVLTSVAISS ALHKKGKLDM VHIQNATPAG GVAVGTAAEM MLMPYGALIV
     GFVCGIISTL GFVYLTPFLE SRLHIQDTCG INNLHGIPGI IGGIVGAVTA ASASLEVYGK
     EGLVHSFDFQ GFKRDWTART QGKFQIYGLL VTLAMALMGG IIVGVGLILR LPFWGQPSDE
     NCFEDAVYWE MPEGNSTVYI PEDPTFKPSG PSVPSVPMVS PLPMASSVPL VP
 
 
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