General Information of Drug Therapeutic Target (DTT) (ID: TTQLO2H)

DTT Name HUMAN C5a receptor (C5aR)
Synonyms CD88; C5aR; C5a-R; C5a anaphylatoxin chemotactic receptor 1; C5R1
Gene Name C5AR1
BioChemical Class
GPCR rhodopsin
UniProt ID
C5AR1_HUMAN
TTD ID
T94912
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MDSFNYTTPDYGHYDDKDTLDLNTPVDKTSNTLRVPDILALVIFAVVFLVGVLGNALVVW
VTAFEAKRTINAIWFLNLAVADFLSCLALPILFTSIVQHHHWPFGGAACSILPSLILLNM
YASILLLATISADRFLLVFKPIWCQNFRGAGLAWIACAVAWGLALLLTIPSFLYRVVREE
YFPPKVLCGVDYSHDKRRERAVAIVRLVLGFLWPLLTLTICYTFILLRTWSRRATRSTKT
LKVVVAVVASFFIFWLPYQVTGIMMSFLEPSSPTFLLLKKLDSLCVSFAYINCCINPIIY
VVAGQGFQGRLRKSLPSLLRNVLTEESVVRESKSFTRSTVDTMAQKTQAV
Function
The ligand interacts with at least two sites on the receptor: a high-affinity site on the extracellular N-terminus, and a second site in the transmembrane region which activates downstream signaling events. Receptor activation stimulates chemotaxis, granule enzyme release, intracellular calcium release and superoxide anion production. Receptor for the chemotactic and inflammatory peptide anaphylatoxin C5a.
KEGG Pathway
Neuroactive ligand-receptor interaction (hsa04080 )
Complement and coagulation cascades (hsa04610 )
Neutrophil extracellular trap formation (hsa04613 )
Alcoholic liver disease (hsa04936 )
Staphylococcus aureus infection (hsa05150 )
Coronavirus disease - COVID-19 (hsa05171 )
Reactome Pathway
G alpha (i) signalling events (R-HSA-418594 )
Neutrophil degranulation (R-HSA-6798695 )
Regulation of Complement cascade (R-HSA-977606 )
Peptide ligand-binding receptors (R-HSA-375276 )

Molecular Interaction Atlas (MIA) of This DTT

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTT
1 Drugs in Phase 2 Trial Targeting This DTT
Drug Name Drug ID Indication ICD 11 Highest Status REF
Avdoralimab DMLAOHX Coronavirus Disease 2019 (COVID-19) 1D6Y Phase 2 Trial [1]
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References

1 Blockade of the C5a-C5aR axis alleviates lung damage in hDPP4-transgenic mice infected with MERS-CoV. Emerg Microbes Infect. 2018 Apr 24;7(1):77.