Swiss-Prot entry
ID PPAR_CAVPO STANDARD; PRT; 467 AA.
AC O35507;
DT 15-JUL-1998 (Rel. 36, Created)
DT 15-JUL-1998 (Rel. 36, Last sequence update)
DT 01-MAY-2005 (Rel. 47, Last annotation update)
DE Peroxisome proliferator activated receptor alpha (PPAR-alpha).
GN Name=PPARA; Synonyms=NR1C1;
OS Cavia porcellus (Guinea pig).
OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
OC Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia;
OC Hystricognathi; Caviidae; Cavia.
OX NCBI_TaxID=10141;
RN [1]
RP NUCLEOTIDE SEQUENCE.
RC STRAIN=Dunkin-Hartley; TISSUE=Liver;
RX MEDLINE=98178962; PubMed=9520140 [NCBI, ExPASy, EBI, Israel, Japan];
RA Tugwood J.D., Holden P.R., James N.H., Prince R.A., Roberts R.A.;
RT "A peroxisome proliferator-activated receptor-alpha (PPARalpha) cDNA
RT cloned from guinea-pig liver encodes a protein with similar properties
RT to the mouse PPARalpha: implications for species differences in
RT responses to peroxisome proliferators.";
RL Arch. Toxicol. 72:169-177(1998).
CC -!- FUNCTION: Receptor that binds peroxisome proliferators such as
CC hypolipidemic drugs and fatty acids. Once activated by a ligand,
CC the receptor binds to a promoter element in the gene for acyl-CoA
CC oxidase and activates its transcription. It therefore controls the
CC peroxisomal beta-oxidation pathway of fatty acids (By similarity).
CC -!- SUBUNIT: Heterodimer with the retinoid X receptor. Interacts with
CC NCOA3 and NCOA6 coactivators, leading to a strong increase of
CC transcription of target genes (By similarity).
CC -!- SUBCELLULAR LOCATION: Nuclear.
CC -!- SIMILARITY: Belongs to the nuclear hormone receptor family. NR1
CC subfamily.
CC -!- SIMILARITY: Contains 1 nuclear receptor DNA-binding domain.
CC --------------------------------------------------------------------------
CC This Swiss-Prot entry is copyright. It is produced through a collaboration
CC between the Swiss Institute of Bioinformatics and the EMBL outstation -
CC the European Bioinformatics Institute. There are no restrictions on its
CC use as long as its content is in no way modified and this statement is not
CC removed.
CC --------------------------------------------------------------------------
DR EMBL; AJ000222; CAA03951.1; -. [EMBL / GenBank / DDBJ] [CoDingSequence]
DR HSSP; Q07869; 1I7G. [HSSP ENTRY / SWISS-3DIMAGE / PDB]
DR SMR; O35507; 200-467.
DR InterPro; IPR000536; Hrmon_recept_lig.
DR InterPro; IPR001723; Stdhrmn_receptor.
DR InterPro; IPR008946; Str_ncl_receptor.
DR InterPro; IPR001628; Znf_C4steroid.
DR InterPro; Graphical view of domain structure.
DR Pfam; PF00104; Hormone_recep; 1.
DR Pfam; PF00105; zf-C4; 1.
DR Pfam; Graphical view of domain structure.
DR PRINTS; PR01288; PROXISOMEPAR.
DR PRINTS; PR01289; PROXISOMPAAR.
DR PRINTS; PR00398; STRDHORMONER.
DR PRINTS; PR00047; STROIDFINGER.
DR ProDom; PD000035; Znf_C4steroid; 1.
DR ProDom [Domain structure / List of seq. sharing at least 1 domain ]
DR SMART; SM00430; HOLI; 1.
DR SMART; SM00399; ZnF_C4; 1.
DR PROSITE; PS00031; NUCLEAR_REC_DBD_1; 1.
DR PROSITE; PS51030; NUCLEAR_REC_DBD_2; 1.
DR HOVERGEN [Family / Alignment / Tree]
DR BLOCKS; O35507.
DR ProtoNet; O35507.
DR ProtoMap; O35507.
DR PRESAGE; O35507.
DR DIP; O35507.
DR ModBase; O35507.
DR SWISS-2DPAGE; GET REGION ON 2D PAGE.
KW Activator; DNA-binding; Multigene family; Nuclear protein; Receptor;
KW Transcription; Transcription regulation; Zinc-finger.
FT DNA_BIND 99 173 Nuclear receptor-type.
FT ZN_FING 102 122 C4-type.
FT ZN_FING 139 161 C4-type.
FT DOMAIN 281 467 Ligand-binding (Potential).
SQ SEQUENCE 467 AA; 52313 MW; D55DD2A6ED0205DE CRC64;
MVDMESPLCP LSPLEAEDLE SPLSEYFLQE MGTIQDISRS LGEDSSGSFG FPEYQYLGSG
PGSDGSVITD TLSPASSPSS VSYPEVPCGV DEPPSSALNI ECRICGDKAS GYHYGVHACE
GCKGFFRRTI RLKLVYDKCD RSCKIQKKNR NKCQYCRFHK CLSVGMSHNA IRFGRMPRSE
KAKLKAEVLT CDRDSEGAET ADLKSLAKRI YEAYLKNFHM NKVKARIILA GKTSSHPLFV
IHDMETLCTA EKTLMAKVVS DGIRDKEAEV RIFHCCQCVS VETVTNLTEF AKAIPGFASL
DLNDQVTLLK YGVYEAIFTM LSSTMNKDGM LVAYGHGFIT REFLKNLRKP FCDMMEPKFN
FAMKFNALEL DDSDISLFVA AIICCGDRPG LLNIDHIEKM QEAIVHVLKL HLQSNHPDDT
FLFPKLLQKL ADLRQLVTEH AQLVQVIKTE SDAALHPLLQ EIYRDMY
//