LPHN1
Изглед
Latrofilin 1 | |||||||||||
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Identifikatori | |||||||||||
Simboli | LPHN1; CIRL1; CL1; LEC2 | ||||||||||
Vanjski ID | MGI: 1929461 HomoloGene: 8951 IUPHAR: LPHN1 GeneCards: LPHN1 Gene | ||||||||||
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Pregled RNK izražavanja | |||||||||||
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podaci | |||||||||||
Ortolozi | |||||||||||
Vrsta | Čovek | Miš | |||||||||
Entrez | 22859 | 330814 | |||||||||
Ensembl | ENSG00000072071 | ENSMUSG00000013033 | |||||||||
UniProt | O94910 | Q80TR1 | |||||||||
RefSeq (mRNA) | NM_001008701.2 | NM_181039.2 | |||||||||
RefSeq (protein) | NP_001008701.1 | NP_851382.2 | |||||||||
Lokacija (UCSC) |
Chr 19: 14.26 - 14.32 Mb |
Chr 8: 86.42 - 86.47 Mb | |||||||||
PubMed pretraga | [1] | [2] |
Latrofilin-1 je protein koji je kod ljudi kodiran LPHN1 genom.[1][2]
Ovaj protein je član latrofilinske familije G protein spregnutih receptora (GPCR). Latrofilini mogu da učestvuju u ćelijskoj adheziji i u prenosu signala. Endogeno proteolitičko razlaganje unutar cisteinom bogatog GPS (GPCR proteolizno mesto) domena proizvodi dve podjedinice (veliku ekstracelularnu N-terminalnu adhezionu jedinicu i podjedinicu koja je u znatno meri slična sa sekretinskom/kalcitoninskom familijom). Ovi domeni su nekovalentno vezani na ćelijskoj membrani. Latrofilin-1 vezuje neurotoksin iz venuma pauka crna udovica, alfa-latrotoksin.[2]
Reference
[уреди | уреди извор]- ^ Hayflick JS (2001). „A family of heptahelical receptors with adhesion-like domains: a marriage between two super families”. J Recept Signal Transduct Res. 20 (2–3): 119—31. PMID 10994649. doi:10.3109/10799890009150640.
- ^ а б „Entrez Gene: LPHN1 latrophilin 1”.
Literatura
[уреди | уреди извор]- Südhof TC (2001). „alpha-Latrotoxin and its receptors: neurexins and CIRL/latrophilins”. Annu. Rev. Neurosci. 24: 933—62. PMID 11520923. doi:10.1146/annurev.neuro.24.1.933.
- Ushkaryov YA, Volynski KE, Ashton AC (2004). „The multiple actions of black widow spider toxins and their selective use in neurosecretion studies”. Toxicon. 43 (5): 527—42. PMID 15066411. doi:10.1016/j.toxicon.2004.02.008.
- Nagase T; Ishikawa K; Suyama M; et al. (1999). „Prediction of the coding sequences of unidentified human genes. XII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro”. DNA Res. 5 (6): 355—64. PMID 10048485. doi:10.1093/dnares/5.6.355.
- Kreienkamp HJ; Zitzer H; Gundelfinger ED; et al. (2000). „The calcium-independent receptor for alpha-latrotoxin from human and rodent brains interacts with members of the ProSAP/SSTRIP/Shank family of multidomain proteins”. J. Biol. Chem. 275 (42): 32387—90. PMID 10964907. doi:10.1074/jbc.C000490200.
- Strausberg RL; Feingold EA; Grouse LH; et al. (2003). „Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899—903. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899.
- Ota T; Suzuki Y; Nishikawa T; et al. (2004). „Complete sequencing and characterization of 21,243 full-length human cDNAs”. Nat. Genet. 36 (1): 40—5. PMID 14702039. doi:10.1038/ng1285.
- Brill LM; Salomon AR; Ficarro SB; et al. (2004). „Robust phosphoproteomic profiling of tyrosine phosphorylation sites from human T cells using immobilized metal affinity chromatography and tandem mass spectrometry”. Anal. Chem. 76 (10): 2763—72. PMID 15144186. doi:10.1021/ac035352d.
- Bjarnadóttir TK; Fredriksson R; Höglund PJ; et al. (2005). „The human and mouse repertoire of the adhesion family of G-protein-coupled receptors”. Genomics. 84 (1): 23—33. PMID 15203201. doi:10.1016/j.ygeno.2003.12.004.
- Gerhard DS; Wagner L; Feingold EA; et al. (2004). „The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121—7. PMC 528928
. PMID 15489334. doi:10.1101/gr.2596504.