LATS1

LATS1
Estruturas disponíveis
PDBPesquisa Human UniProt: PDBe RCSB
Identificadores
Nomes alternativosLATS1
IDs externosOMIM: 603473 HomoloGene: 55843 GeneCards: LATS1
Número EC2.7.11.1
Wikidata
Ver/Editar Humano

A grande supressora de tumor quinase 1 (LATS1) é uma enzima que em humanos é codificada pelo gene LATS1.[2][3][4]

Ele foi associado à via de sinalização Hippo.[5][6][7]

Interações

O LATS1 demonstrou interagir com Zyxin[8] e Cdk1.[2]

Referências

  1. «Human PubMed Reference:» 
  2. a b Tao W, Zhang S, Turenchalk GS, Stewart RA, St John MA, Chen W, Xu T (fevereiro de 1999). «Human homologue of the Drosophila melanogaster lats tumour suppressor modulates CDC2 activity». Nat Genet. 21 (2): 177–81. PMID 9988268. doi:10.1038/5960 
  3. Iida S, Hirota T, Morisaki T, Marumoto T, Hara T, Kuninaka S, Honda S, Kosai K, Kawasuji M, Pallas DC, Saya H (julho de 2004). «Tumor suppressor WARTS ensures genomic integrity by regulating both mitotic progression and G1 tetraploidy checkpoint function». Oncogene. 23 (31): 5266–74. PMID 15122335. doi:10.1038/sj.onc.1207623 
  4. «Entrez Gene: LATS1 LATS, large tumor suppressor, homolog 1 (Drosophila)» 
  5. Saucedo LJ, Edgar BA (agosto de 2007). «Filling out the Hippo pathway». Nature Reviews. Molecular Cell Biology. 8 (8): 613–21. PMID 17622252. doi:10.1038/nrm2221 
  6. Zhao B, Tumaneng K, Guan KL (agosto de 2011). «The Hippo pathway in organ size control, tissue regeneration and stem cell self-renewal». Nature Cell Biology. 13 (8): 877–83. PMC 3987945Acessível livremente. PMID 21808241. doi:10.1038/ncb2303 
  7. Hao Y, Chun A, Cheung K, Rashidi B, Yang X (fevereiro de 2008). «Tumor suppressor LATS1 is a negative regulator of oncogene YAP». J. Biol. Chem. 283 (9): 5496–509. PMID 18158288. doi:10.1074/jbc.M709037200 
  8. Hirota, T; Morisaki T; Nishiyama Y; Marumoto T; Tada K; Hara T; Masuko N; Inagaki M; Hatakeyama K; Saya H (maio de 2000). «Zyxin, a regulator of actin filament assembly, targets the mitotic apparatus by interacting with h-warts/LATS1 tumor suppressor». J. Cell Biol. 149 (5): 1073–86. ISSN 0021-9525. PMC 2174824Acessível livremente. PMID 10831611. doi:10.1083/jcb.149.5.1073 

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