P2RY4: Difference between revisions

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imported>Ser Amantio di Nicolao
 
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{{Infobox_gene}}
 
'''P2Y purinoceptor 4''' is a [[protein]] that in humans is encoded by the ''P2RY4'' [[gene]].<ref name="pmid8537336">{{cite journal | vauthors = Communi D, Pirotton S, Parmentier M, Boeynaems JM | title = Cloning and functional expression of a human uridine nucleotide receptor | journal = J Biol Chem | volume = 270 | issue = 52 | pages = 30849–52 |date=Feb 1996 | pmid = 8537336 | pmc =  | doi =10.1074/jbc.270.52.30849 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5030| accessdate = }}</ref>
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{{GNF_Protein_box
| image =
| image_source = 
| PDB =
| Name = Pyrimidinergic receptor P2Y, G-protein coupled, 4
| HGNCid = 8542
| Symbol = P2RY4
| AltSymbols =; NRU; P2P; P2Y4; UNR
| OMIM = 300038
| ECnumber = 
| Homologene = 20568
| MGIid = 1926594
| GeneAtlas_image1 = PBB_GE_P2RY4_221466_at_tn.png
| Function = {{GNF_GO|id=GO:0001584 |text = rhodopsin-like receptor activity}} {{GNF_GO|id=GO:0004872 |text = receptor activity}} {{GNF_GO|id=GO:0045030 |text = UTP-activated nucleotide receptor activity}}
| Component = {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0007165 |text = signal transduction}} {{GNF_GO|id=GO:0007200 |text = G-protein signaling, coupled to IP3 second messenger (phospholipase C activating)}} {{GNF_GO|id=GO:0007204 |text = elevation of cytosolic calcium ion concentration}} {{GNF_GO|id=GO:0030321 |text = transepithelial chloride transport}}
  | Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 5030
    | Hs_Ensembl = ENSG00000186912
    | Hs_RefseqProtein = NP_002556
    | Hs_RefseqmRNA = NM_002565
    | Hs_GenLoc_db =   
    | Hs_GenLoc_chr = X
    | Hs_GenLoc_start = 69394745
    | Hs_GenLoc_end = 69396339
    | Hs_Uniprot = P51582
    | Mm_EntrezGene = 57385
    | Mm_Ensembl = ENSMUSG00000044359
    | Mm_RefseqmRNA = NM_020621
    | Mm_RefseqProtein = NP_065646
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = X
    | Mm_GenLoc_start = 96792873
    | Mm_GenLoc_end = 96797588
    | Mm_Uniprot = Q0VBT7
  }}
}}
'''Pyrimidinergic receptor P2Y, G-protein coupled, 4''', also known as '''P2RY4''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5030| accessdate = }}</ref>


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{{PBB_Summary
{{PBB_Summary
| section_title =  
| section_title =  
| summary_text = The product of this gene belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is responsive to uridine nucleotides, partially responsive to ATP, and not responsive to ADP.<ref name="entrez">{{cite web | title = Entrez Gene: P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5030| accessdate = }}</ref>
| summary_text = The product of this gene, P2Y<sub>4</sub>, belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is responsive to uridine nucleotides, partially responsive to ATP, and not responsive to ADP.<ref name="entrez">{{cite web | title = Entrez Gene: P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5030| accessdate = }}</ref>
}}
}}


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==References==
==References==
{{reflist|2}}
{{reflist}}
 
==External links==
*{{cite web | url = http://www.iuphar-db.org/GPCR/ReceptorDisplayForward?receptorID=2396 | title = P2Y Receptors: P2Y<sub>4</sub> | accessdate = | date = | work = IUPHAR Database of Receptors and Ion Channels | publisher = International Union of Basic and Clinical Pharmacology | pages = | archiveurl = | archivedate = }}


==Further reading==
==Further reading==
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{{PBB_Further_reading  
{{PBB_Further_reading  
| citations =  
| citations =  
*{{cite journal | author=Nguyen T, Erb L, Weisman GA, ''et al.'' |title=Cloning, expression, and chromosomal localization of the human uridine nucleotide receptor gene. |journal=J. Biol. Chem. |volume=270 |issue= 52 |pages= 30845-8 |year= 1996 |pmid= 8537335 |doi= }}
*{{cite journal   |vauthors=Nguyen T, Erb L, Weisman GA, etal |title=Cloning, expression, and chromosomal localization of the human uridine nucleotide receptor gene. |journal=J. Biol. Chem. |volume=270 |issue= 52 |pages= 30845–8 |year= 1996 |pmid= 8537335 |doi=10.1074/jbc.270.52.30845 }}
*{{cite journal  | author=Communi D, Pirotton S, Parmentier M, Boeynaems JM |title=Cloning and functional expression of a human uridine nucleotide receptor. |journal=J. Biol. Chem. |volume=270 |issue= 52 |pages= 30849-52 |year= 1996 |pmid= 8537336 |doi= }}
*{{cite journal  | vauthors=Stam NJ, Klomp J, Van de Heuvel N, Olijve W |title=Molecular cloning and characterization of a novel orphan receptor (P2P) expressed in human pancreas that shows high structural homology to the P2U purinoceptor. |journal=FEBS Lett. |volume=384 |issue= 3 |pages= 260–4 |year= 1996 |pmid= 8617367 |doi=10.1016/0014-5793(96)00321-3 }}
*{{cite journal  | author=Stam NJ, Klomp J, Van de Heuvel N, Olijve W |title=Molecular cloning and characterization of a novel orphan receptor (P2P) expressed in human pancreas that shows high structural homology to the P2U purinoceptor. |journal=FEBS Lett. |volume=384 |issue= 3 |pages= 260-4 |year= 1996 |pmid= 8617367 |doi=  }}
*{{cite journal   |vauthors=Nicholas RA, Watt WC, Lazarowski ER, etal |title=Uridine nucleotide selectivity of three phospholipase C-activating P2 receptors: identification of a UDP-selective, a UTP-selective, and an ATP- and UTP-specific receptor. |journal=Mol. Pharmacol. |volume=50 |issue= 2 |pages= 224–9 |year= 1996 |pmid= 8700127 |doi=  }}
*{{cite journal | author=Nicholas RA, Watt WC, Lazarowski ER, ''et al.'' |title=Uridine nucleotide selectivity of three phospholipase C-activating P2 receptors: identification of a UDP-selective, a UTP-selective, and an ATP- and UTP-specific receptor. |journal=Mol. Pharmacol. |volume=50 |issue= 2 |pages= 224-9 |year= 1996 |pmid= 8700127 |doi=  }}
*{{cite journal  | vauthors=Maier R, Glatz A, Mosbacher J, Bilbe G |title=Cloning of P2Y6 cDNAs and identification of a pseudogene: comparison of P2Y receptor subtype expression in bone and brain tissues. |journal=Biochem. Biophys. Res. Commun. |volume=237 |issue= 2 |pages= 297–302 |year= 1997 |pmid= 9268704 |doi= 10.1006/bbrc.1997.7135 }}
*{{cite journal  | author=Maier R, Glatz A, Mosbacher J, Bilbe G |title=Cloning of P2Y6 cDNAs and identification of a pseudogene: comparison of P2Y receptor subtype expression in bone and brain tissues. |journal=Biochem. Biophys. Res. Commun. |volume=237 |issue= 2 |pages= 297-302 |year= 1997 |pmid= 9268704 |doi= 10.1006/bbrc.1997.7135 }}
*{{cite journal  | vauthors=Jin J, Dasari VR, Sistare FD, Kunapuli SP |title=Distribution of P2Y receptor subtypes on haematopoietic cells. |journal=Br. J. Pharmacol. |volume=123 |issue= 5 |pages= 789–94 |year= 1998 |pmid= 9535005 |doi= 10.1038/sj.bjp.0701665 | pmc=1565225 }}
*{{cite journal  | author=Jin J, Dasari VR, Sistare FD, Kunapuli SP |title=Distribution of P2Y receptor subtypes on haematopoietic cells. |journal=Br. J. Pharmacol. |volume=123 |issue= 5 |pages= 789-94 |year= 1998 |pmid= 9535005 |doi= 10.1038/sj.bjp.0701665 }}
*{{cite journal  | vauthors=Brinson AE, Harden TK |title=Differential regulation of the uridine nucleotide-activated P2Y4 and P2Y6 receptors. SER-333 and SER-334 in the carboxyl terminus are involved in agonist-dependent phosphorylation desensitization and internalization of the P2Y4 receptor. |journal=J. Biol. Chem. |volume=276 |issue= 15 |pages= 11939–48 |year= 2001 |pmid= 11114308 |doi= 10.1074/jbc.M009909200 }}
*{{cite journal  | author=Brinson AE, Harden TK |title=Differential regulation of the uridine nucleotide-activated P2Y4 and P2Y6 receptors. SER-333 and SER-334 in the carboxyl terminus are involved in agonist-dependent phosphorylation desensitization and internalization of the P2Y4 receptor. |journal=J. Biol. Chem. |volume=276 |issue= 15 |pages= 11939-48 |year= 2001 |pmid= 11114308 |doi= 10.1074/jbc.M009909200 }}
*{{cite journal  | vauthors=Suarez-Huerta N, Pouillon V, Boeynaems J, Robaye B |title=Molecular cloning and characterization of the mouse P2Y4 nucleotide receptor. |journal=Eur. J. Pharmacol. |volume=416 |issue= 3 |pages= 197–202 |year= 2001 |pmid= 11290369 |doi=10.1016/S0014-2999(01)00875-5 }}
*{{cite journal  | author=Suarez-Huerta N, Pouillon V, Boeynaems J, Robaye B |title=Molecular cloning and characterization of the mouse P2Y4 nucleotide receptor. |journal=Eur. J. Pharmacol. |volume=416 |issue= 3 |pages= 197-202 |year= 2001 |pmid= 11290369 |doi=  }}
*{{cite journal   |vauthors=Moore DJ, Chambers JK, Wahlin JP, etal |title=Expression pattern of human P2Y receptor subtypes: a quantitative reverse transcription-polymerase chain reaction study. |journal=Biochim. Biophys. Acta |volume=1521 |issue= 1-3 |pages= 107–19 |year= 2001 |pmid= 11690642 |doi=  10.1016/S0167-4781(01)00291-3}}
*{{cite journal | author=Moore DJ, Chambers JK, Wahlin JP, ''et al.'' |title=Expression pattern of human P2Y receptor subtypes: a quantitative reverse transcription-polymerase chain reaction study. |journal=Biochim. Biophys. Acta |volume=1521 |issue= 1-3 |pages= 107-19 |year= 2001 |pmid= 11690642 |doi=  }}
*{{cite journal   |vauthors=Idzko M, Dichmann S, Ferrari D, etal |title=Nucleotides induce chemotaxis and actin polymerization in immature but not mature human dendritic cells via activation of pertussis toxin-sensitive P2y receptors. |journal=Blood |volume=100 |issue= 3 |pages= 925–32 |year= 2002 |pmid= 12130504 |doi=10.1182/blood.V100.3.925 }}
*{{cite journal | author=Idzko M, Dichmann S, Ferrari D, ''et al.'' |title=Nucleotides induce chemotaxis and actin polymerization in immature but not mature human dendritic cells via activation of pertussis toxin-sensitive P2y receptors. |journal=Blood |volume=100 |issue= 3 |pages= 925-32 |year= 2002 |pmid= 12130504 |doi=  }}
*{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal  | vauthors=Burrell HE, Bowler WB, Gallagher JA, Sharpe GR |title=Human keratinocytes express multiple P2Y-receptors: evidence for functional P2Y1, P2Y2, and P2Y4 receptors. |journal=J. Invest. Dermatol. |volume=120 |issue= 3 |pages= 440–7 |year= 2003 |pmid= 12603858 |doi= 10.1046/j.1523-1747.2003.12050.x }}
*{{cite journal  | author=Burrell HE, Bowler WB, Gallagher JA, Sharpe GR |title=Human keratinocytes express multiple P2Y-receptors: evidence for functional P2Y1, P2Y2, and P2Y4 receptors. |journal=J. Invest. Dermatol. |volume=120 |issue= 3 |pages= 440-7 |year= 2003 |pmid= 12603858 |doi= 10.1046/j.1523-1747.2003.12050.x }}
*{{cite journal   |vauthors=Kim SG, Soltysiak KA, Gao ZG, etal |title=Tumor necrosis factor alpha-induced apoptosis in astrocytes is prevented by the activation of P2Y6, but not P2Y4 nucleotide receptors. |journal=Biochem. Pharmacol. |volume=65 |issue= 6 |pages= 923–31 |year= 2003 |pmid= 12623123 |doi=10.1016/S0006-2952(02)01614-3 |pmc=3402349}}
*{{cite journal | author=Kim SG, Soltysiak KA, Gao ZG, ''et al.'' |title=Tumor necrosis factor alpha-induced apoptosis in astrocytes is prevented by the activation of P2Y6, but not P2Y4 nucleotide receptors. |journal=Biochem. Pharmacol. |volume=65 |issue= 6 |pages= 923-31 |year= 2003 |pmid= 12623123 |doi= }}
*{{cite journal  | vauthors=Herold CL, Qi AD, Harden TK, Nicholas RA |title=Agonist versus antagonist action of ATP at the P2Y4 receptor is determined by the second extracellular loop. |journal=J. Biol. Chem. |volume=279 |issue= 12 |pages= 11456–64 |year= 2004 |pmid= 14670966 |doi= 10.1074/jbc.M301734200 | pmc=1821344 }}
*{{cite journal  | author=Herold CL, Qi AD, Harden TK, Nicholas RA |title=Agonist versus antagonist action of ATP at the P2Y4 receptor is determined by the second extracellular loop. |journal=J. Biol. Chem. |volume=279 |issue= 12 |pages= 11456-64 |year= 2004 |pmid= 14670966 |doi= 10.1074/jbc.M301734200 }}
*{{cite journal   |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal   |vauthors=Cavaliere F, Nestola V, Amadio S, etal |title=The metabotropic P2Y4 receptor participates in the commitment to differentiation and cell death of human neuroblastoma SH-SY5Y cells. |journal=Neurobiol. Dis. |volume=18 |issue= 1 |pages= 100–9 |year= 2005 |pmid= 15649700 |doi= 10.1016/j.nbd.2004.09.001 }}
*{{cite journal | author=Cavaliere F, Nestola V, Amadio S, ''et al.'' |title=The metabotropic P2Y4 receptor participates in the commitment to differentiation and cell death of human neuroblastoma SH-SY5Y cells. |journal=Neurobiol. Dis. |volume=18 |issue= 1 |pages= 100-9 |year= 2005 |pmid= 15649700 |doi= 10.1016/j.nbd.2004.09.001 }}
*{{cite journal   |vauthors=Ross MT, Grafham DV, Coffey AJ, etal |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440 | pmc=2665286 }}
*{{cite journal | author=Ross MT, Grafham DV, Coffey AJ, ''et al.'' |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325-37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440 }}
}}
}}
{{refend}}
{{refend}}
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{{NLM content}}
{{NLM content}}
{{G protein-coupled receptors}}
{{G protein-coupled receptors}}
[[Category:G protein coupled receptors]]
{{Purinergics}}
 
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{{WH}}
[[Category:G protein-coupled receptors]]
{{WS}}
{{transmembranereceptor-stub}}

Latest revision as of 18:01, 24 September 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

P2Y purinoceptor 4 is a protein that in humans is encoded by the P2RY4 gene.[1][2]

The product of this gene, P2Y4, belongs to the family of G-protein coupled receptors. This family has several receptor subtypes with different pharmacological selectivity, which overlaps in some cases, for various adenosine and uridine nucleotides. This receptor is responsive to uridine nucleotides, partially responsive to ATP, and not responsive to ADP.[2]

See also

References

  1. Communi D, Pirotton S, Parmentier M, Boeynaems JM (Feb 1996). "Cloning and functional expression of a human uridine nucleotide receptor". J Biol Chem. 270 (52): 30849–52. doi:10.1074/jbc.270.52.30849. PMID 8537336.
  2. 2.0 2.1 "Entrez Gene: P2RY4 pyrimidinergic receptor P2Y, G-protein coupled, 4".

External links

  • "P2Y Receptors: P2Y4". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.