PTK6

Today, PTK6 is a topic that arouses great interest and debate in society. Since its origins, PTK6 has captured the attention of people of all ages, cultures and contexts, becoming a frequent topic of conversation both professionally and personally. Over time, PTK6 has evolved in various ways and has acquired a relevant role in different aspects of daily life. Thus, it is essential to analyze and understand PTK6 in depth, its implications and its impact on today's society. In this article, we will delve into the world of PTK6 to address its many facets and offer a broad and enriching vision of this topic that is so relevant today.

PTK6
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesPTK6, BRK, protein tyrosine kinase 6
External IDsOMIM: 602004; MGI: 99683; HomoloGene: 68494; GeneCards: PTK6; OMA:PTK6 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001256358
NM_005975

NM_009184
NM_001356304

RefSeq (protein)

NP_001243287
NP_005966

NP_033210
NP_001343233

Location (UCSC)Chr 20: 63.53 – 63.54 MbChr 2: 180.84 – 180.84 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Tyrosine-protein kinase 6 is an enzyme that in humans is encoded by the PTK6 gene.[5][6][7]

Function

Tyrosine-protein kinase 6—also known as BRK[7] (breast tumor kinase)—is a cytoplasmic non-receptor protein kinase which may function as an intracellular signal transducer in epithelial tissues. The encoded protein has been shown to undergo autophosphorylation.[7]

Clinical significance

Overexpression of this gene in mammary epithelial cells leads to sensitization of the cells to epidermal growth factor and results in a partially transformed phenotype. Expression of this gene has been detected at low levels in some breast tumors but not in normal breast tissue.[7]

Interactions

PTK6 has been shown to interact with STAP2[8] and KHDRBS1.[9]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000101213Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000038751Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lee ST, Strunk KM, Spritz RA (December 1993). "A survey of protein tyrosine kinase mRNAs expressed in normal human melanocytes". Oncogene. 8 (12): 3403–10. PMID 8247543.
  6. ^ Park SH, Lee KH, Kim H, Lee ST (September 1997). "Assignment of the human PTK6 gene encoding a non-receptor protein tyrosine kinase to 20q13.3 by fluorescence in situ hybridization". Cytogenet Cell Genet. 77 (3–4): 271–2. doi:10.1159/000134595. PMID 9284935.
  7. ^ a b c d "PTK6 protein tyrosine kinase 6". National Center for Biotechnology Information (NCBI). 4 June 2020.
  8. ^ Mitchell PJ, Sara E A, Crompton M R (August 2000). "A novel adaptor-like protein which is a substrate for the non-receptor tyrosine kinase, BRK". Oncogene. 19 (37). ENGLAND: 4273–82. doi:10.1038/sj.onc.1203775. ISSN 0950-9232. PMID 10980601.
  9. ^ Derry JJ, Richard S, Valderrama Carvajal H, Ye X, Vasioukhin V, Cochrane A W, Chen T, Tyner A L (August 2000). "Sik (BRK) Phosphorylates Sam68 in the Nucleus and Negatively Regulates Its RNA Binding Ability". Mol. Cell. Biol. 20 (16). UNITED STATES: 6114–26. doi:10.1128/MCB.20.16.6114-6126.2000. ISSN 0270-7306. PMC 86087. PMID 10913193.

Further reading