Description: Homo sapiens ADCYAP receptor type I (ADCYAP1R1), transcript variant 3, mRNA. (from RefSeq NM_001118) RefSeq Summary (NM_001118): This gene encodes type I adenylate cyclase activating polypeptide receptor, which is a membrane-associated protein and shares significant homology with members of the glucagon/secretin receptor family. This receptor mediates diverse biological actions of adenylate cyclase activating polypeptide 1 and is positively coupled to adenylate cyclase. Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified. [provided by RefSeq, Dec 2010]. Gencode Transcript: ENST00000304166.9 Gencode Gene: ENSG00000078549.15 Transcript (Including UTRs) Position: hg38 chr7:31,052,308-31,111,474 Size: 59,167 Total Exon Count: 16 Strand: + Coding Region Position: hg38 chr7:31,063,265-31,106,684 Size: 43,420 Coding Exon Count: 15
ID:PACR_HUMAN DESCRIPTION: RecName: Full=Pituitary adenylate cyclase-activating polypeptide type I receptor; Short=PACAP type I receptor; Short=PACAP-R-1; Short=PACAP-R1; Flags: Precursor; FUNCTION: This is a receptor for PACAP-27 and PACAP-38. The activity of this receptor is mediated by G proteins which activate adenylyl cyclase. May regulate the release of adrenocorticotropin, luteinizing hormone, growth hormone, prolactin, epinephrine, and catecholamine. May play a role in spermatogenesis and sperm motility. Causes smooth muscle relaxation and secretion in the gastrointestinal tract. SUBUNIT: Interacts (via N-terminal extracellular domain) with ADCYAP1. SUBCELLULAR LOCATION: Cell membrane; Multi-pass membrane protein. TISSUE SPECIFICITY: Most abundant in the brain, low expression in the lung, liver, thymus, spleen, pancreas and placenta. SIMILARITY: Belongs to the G-protein coupled receptor 2 family. SEQUENCE CAUTION: Sequence=BAA04466.1; Type=Erroneous initiation;
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on P41586
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Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.