DRD1
D(1A) dopamine receptor
Also known as: DRD1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P21728
- Gene
- DRD1
- Ensembl
- ENSG00000184845
- Chromosome
- 5
- Canonical length
- 446 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted membrane proteins
- Subcellular location
- Plasma membrane,Cytosol
OverviewNCBI Gene
This gene encodes the D1 subtype of the dopamine receptor. The D1 subtype is the most abundant dopamine receptor in the central nervous system. This G-protein coupled receptor stimulates adenylyl cyclase and activates cyclic AMP-dependent protein kinases. D1 receptors regulate neuronal growth and development, mediate some behavioral responses, and modulate dopamine receptor D2-mediated events. Alternate transcription initiation sites result in two transcript variants of this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
446 residues, UniProt reviewed canonical sequence.
>P21728|DRD1
1 MRTLNTSAMD GTGLVVERDF SVRILTACFL SLLILSTLLG NTLVCAAVIR FRHLRSKVTN
61 FFVISLAVSD LLVAVLVMPW KAVAEIAGFW PFGSFCNIWV AFDIMCSTAS ILNLCVISVD
121 RYWAISSPFR YERKMTPKAA FILISVAWTL SVLISFIPVQ LSWHKAKPTS PSDGNATSLA
181 ETIDNCDSSL SRTYAISSSV ISFYIPVAIM IVTYTRIYRI AQKQIRRIAA LERAAVHAKN
241 CQTTTGNGKP VECSQPESSF KMSFKRETKV LKTLSVIMGV FVCCWLPFFI LNCILPFCGS
301 GETQPFCIDS NTFDVFVWFG WANSSLNPII YAFNADFRKA FSTLLGCYRL CPATNNAIET
361 VSINNNGAAM FSSHHEPRGS ISKECNLVYL IPHAVGSSED LKKEEAAGIA RPLEKLSPAL
421 SVILDYDTDV SLEKIQPITQ NGQHPTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against DRD1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.43
- Highest tissue expression
- 26 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 26 nTPM
- retina: 7.8 nTPM
- cerebral cortex: 4.6 nTPM
- amygdala: 2.4 nTPM
- hippocampal formation: 1.6 nTPM
- hypothalamus: 1.2 nTPM
Single-cell type
- retinal amacrine cells: 34 nCPM
- retinal horizontal cells: 32 nCPM
- brain inhibitory neurons: 32 nCPM
- retinal bipolar cells: 21 nCPM
- ependymal cells: 18 nCPM
- vascular smooth muscle cells: 6.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 47 nTPM
- cerebral cortex: 12 nTPM
- white matter: 6.9 nTPM
- amygdala: 6.8 nTPM
- thalamus: 4.1 nTPM
- hippocampal formation: 3.7 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.31
- gnomAD pLI
- 0.96
- gnomAD missense Z
- 2.26
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adenylate cyclase-activating adrenergic receptor signaling pathway
- adenylate cyclase-activating dopamine receptor signaling pathway
- adenylate cyclase-activating G protein-coupled receptor signaling pathway
- adult walking behavior
- astrocyte development
- behavioral fear response
- behavioral response to cocaine
- cellular response to catecholamine stimulus
- cerebral cortex GABAergic interneuron migration
- conditioned taste aversion
- D-glucose import
- dentate gyrus development
- dopamine metabolic process
- dopamine transport
- G protein-coupled dopamine receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- grooming behavior
- habituation
- long-term synaptic depression
- long-term synaptic potentiation
- maternal behavior
- mating behavior
- memory
- modification of postsynaptic structure
- neuronal action potential
- operant conditioning
- peristalsis
- phospholipase C-activating dopamine receptor signaling pathway
- positive regulation of cell migration
- positive regulation of MAPK cascade
- positive regulation of neuron migration
- positive regulation of potassium ion transport
- positive regulation of release of sequestered calcium ion into cytosol
- positive regulation of synaptic transmission, glutamatergic
- presynaptic modulation of chemical synaptic transmission
- protein import into nucleus
- regulation of dopamine metabolic process
- regulation of dopamine uptake involved in synaptic transmission
- response to amphetamine
- response to xenobiotic stimulus
- sensitization
- striatum development
- synapse assembly
- synaptic transmission, glutamatergic
- temperature homeostasis
- transmission of nerve impulse
- vasodilation
- visual learning
Molecular functions
- arrestin family protein binding
- dopamine binding
- dopamine neurotransmitter receptor activity
- dopamine neurotransmitter receptor activity, coupled via Gs
- G protein-coupled receptor activity
- G-protein alpha-subunit binding
- heterotrimeric G-protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of DRD1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads DRD1 as an antibody target. Whether an autoantibody or antibody against DRD1 could matter depends on whether native DRD1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
DRD1 is annotated at the cell surface, where native DRD1 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label DRD1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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