LPAR1

Receptor lizofosfatidne kiseline 1
Identifikatori
Simboli LPAR1; EDG2; LPA1; Mrec1.3; VZG1; edg-2; rec.1.3; vzg-1
Vanjski ID OMIM602282 MGI108429 HomoloGene1072 IUPHAR: LPA1 GeneCards: LPAR1 Gene
Pregled RNK izražavanja
podaci
Ortolozi
Vrsta Čovek Miš
Entrez 1902 14745
Ensembl ENSG00000198121 ENSMUSG00000038668
UniProt Q92633 P61793
RefSeq (mRNA) NM_001401.3 NM_010336.2
RefSeq (protein) NP_001392.2 NP_034466.2
Lokacija (UCSC) Chr 9:
113.64 - 113.8 Mb
Chr 4:
58.45 - 58.57 Mb
PubMed pretraga [1] [2]

Receptor lizofosfatidne kiseline 1 (LPA1) je protein koji je kod ljudi kodiran LPAR1 genom.[1][2][3] LPA1 je G protein spregnuti receptor za koji se vezuje lipidni signalni molekul lizofosfatidna kiselina (LPA).[4]

Funkcija

Integralni membranski protein kodiran ovim genom pripada grupi EDG receptora. Ti receptori su članovi familije G protein spregnutih receptora. EDG receptori posreduju različite bioločkie funkcije, uključujući proliferaciju, agregaciju trombocita, kontrakcije glatkih mišića, inhibiciju diferencijaciju neuroblastomnih ćelija, hemotaksu, i invaziju tumornih ćelija. Alternativno splajsovanje ovog gena je uočeno i dve transkriptne varijante su opisane. One kodiraju identične proteine.[1]

Reference

  1. ^ а б „Entrez Gene: LPAR1 Lysophosphatidic acid receptor 1”. 
  2. ^ Hecht JH, Weiner JA, Post SR, Chun J (1996). „Ventricular zone gene-1 (vzg-1) encodes a lysophosphatidic acid receptor expressed in neurogenic regions of the developing cerebral cortex”. J. Cell Biol.. 135 (4): 1071—83. PMC 2133395Слободан приступ. PMID 8922387. doi:10.1083/jcb.135.4.1071. 
  3. ^ An S, Dickens MA, Bleu T, Hallmark OG, Goetzl EJ (1997). „Molecular cloning of the human Edg2 protein and its identification as a functional cellular receptor for lysophosphatidic acid”. Biochem. Biophys. Res. Commun.. 231 (3): 619—22. PMID 9070858. doi:10.1006/bbrc.1997.6150. 
  4. ^ Choi JW, Herr DR, Noguchi K, Yung YC, Lee CW, Mutoh T, Lin ME, Teo ST, Park KE, Mosley AN, Chun J (2010). „LPA Receptors: Subtypes and Biological Actions”. Annual Review of Pharmacology and Toxicology. 50 (1): 157—186. PMID 20055701. doi:10.1146/annurev.pharmtox.010909.105753. 

Literatura

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