Homo sapiens (human): 5733
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Entry
5733 CDS
T01001
Symbol
PTGER3, EP3, EP3-I, EP3-II, EP3-III, EP3-IV, EP3-VI, EP3e, PGE2-R, lnc003875
Name
(RefSeq) prostaglandin E receptor 3
KO
K04260
prostaglandin E receptor 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04020
Calcium signaling pathway
hsa04024
cAMP signaling pathway
hsa04080
Neuroactive ligand-receptor interaction
hsa04923
Regulation of lipolysis in adipocytes
hsa05163
Human cytomegalovirus infection
hsa05200
Pathways in cancer
Network
nt06528
Calcium signaling
Element
N01640
GPCR-PLCB-ITPR signaling pathway
Drug target
Enprostil:
D01891
Misoprostol:
D00419
<JP/US>
Sepetaprost:
D12617
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04024 cAMP signaling pathway
5733 (PTGER3)
09133 Signaling molecules and interaction
04080 Neuroactive ligand-receptor interaction
5733 (PTGER3)
09150 Organismal Systems
09152 Endocrine system
04923 Regulation of lipolysis in adipocytes
5733 (PTGER3)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
5733 (PTGER3)
09172 Infectious disease: viral
05163 Human cytomegalovirus infection
5733 (PTGER3)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
04030 G protein-coupled receptors [BR:
hsa04030
]
5733 (PTGER3)
G protein-coupled receptors [BR:
hsa04030
]
Rhodopsin family
Lipid
Prostaglandin
5733 (PTGER3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
7tm_1
7TM_GPCR_Srx
ECF_trnsprt
Motif
Other DBs
NCBI-GeneID:
5733
NCBI-ProteinID:
NP_001119516
OMIM:
176806
HGNC:
9595
Ensembl:
ENSG00000050628
UniProt:
P43115
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(70852358..71047816)
Genome browser
AA seq
390 aa
AA seq
DB search
MKETRGYGGDAPFCTRLNHSYTGMWAPERSAEARGNLTRPPGSGEDCGSVSVAFPITMLL
TGFVGNALAMLLVSRSYRRRESKRKKSFLLCIGWLALTDLVGQLLTTPVVIVVYLSKQRW
EHIDPSGRLCTFFGLTMTVFGLSSLFIASAMAVERALAIRAPHWYASHMKTRATRAVLLG
VWLAVLAFALLPVLGVGQYTVQWPGTWCFISTGRGGNGTSSSHNWGNLFFASAFAFLGLL
ALTVTFSCNLATIKALVSRCRAKATASQSSAQWGRITTETAIQLMGIMCVLSVCWSPLLI
MMLKMIFNQTSVEHCKTHTEKQKECNFFLIAVRLASLNQILDPWVYLLLRKILLRKFCQI
RYHTNNYASSSTSLPCQCSSTLMWSDHLER
NT seq
1173 nt
NT seq
+upstream
nt +downstream
nt
atgaaggagacccggggctacggaggggatgcccccttctgcacccgcctcaaccactcc
tacacaggcatgtgggcgcccgagcgttccgccgaggcgcggggcaacctcacgcgccct
ccagggtctggcgaggattgcggatcggtgtccgtggccttcccgatcaccatgctgctc
actggtttcgtgggcaacgcactggccatgctgctcgtgtcgcgcagctaccggcgccgg
gagagcaagcgcaagaagtccttcctgctgtgcatcggctggctggcgctcaccgacctg
gtcgggcagcttctcaccaccccggtcgtcatcgtcgtgtacctgtccaagcagcgttgg
gagcacatcgacccgtcggggcggctctgcacctttttcgggctgaccatgactgttttc
gggctctcctcgttgttcatcgccagcgccatggccgtcgagcgggcgctggccatcagg
gcgccgcactggtatgcgagccacatgaagacgcgtgccacccgcgctgtgctgctcggc
gtgtggctggccgtgctcgccttcgccctgctgccggtgctgggcgtgggccagtacacc
gtccagtggcccgggacgtggtgcttcatcagcaccgggcgagggggcaacgggactagc
tcttcgcataactggggcaaccttttcttcgcctctgcctttgccttcctggggctcttg
gcgctgacagtcaccttttcctgcaacctggccaccattaaggccctggtgtcccgctgc
cgggccaaggccacggcatctcagtccagtgcccagtggggccgcatcacgaccgagacg
gccattcagcttatggggatcatgtgcgtgctgtcggtctgctggtctccgctcctgata
atgatgttgaaaatgatcttcaatcagacatcagttgagcactgcaagacacacacggag
aagcagaaagaatgcaacttcttcttaatagctgttcgcctggcttcactgaaccagatc
ttggatccttgggtttacctgctgttaagaaagatccttcttcgaaagttttgccagatc
aggtaccacacaaacaactatgcatccagctccacctccttaccctgccagtgttcctca
accttgatgtggagcgaccatttggaaagatga
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